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Melissa A Heitmann

age ~45

from Hopewell Junction, NY

Also known as:
  • Melissa A Simmerly
  • Melissa A Heitman
Phone and address:
8 E Hook Cross Rd, East Fishkill, NY 12533

Melissa Heitmann Phones & Addresses

  • 8 E Hook Cross Rd, Hopewell Jct, NY 12533
  • Hopewell Junction, NY
  • West Oneonta, NY
  • Vernon Rockville, CT
  • Middletown, CT
  • Troy, NY
  • Vernon Rockvl, CT

Work

  • Company:
    Mannkind corporation
    Jan 1, 2007
  • Position:
    Process engineer

Education

  • Degree:
    Bachelors, Bachelor of Science
  • School / High School:
    Rensselaer Polytechnic Institute
    1997 to 2001
  • Specialities:
    Chemical Engineering

Industries

Pharmaceuticals

Us Patents

  • Formation Of N-Protected Bis-3,6-(4-Aminoalkyl)-2,5,Diketopiperazine

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  • US Patent:
    20130012710, Jan 10, 2013
  • Filed:
    Feb 7, 2012
  • Appl. No.:
    13/368172
  • Inventors:
    John J. Freeman - New Fairfield CT, US
    Adrienne Stamper - Naugatuck CT, US
    Melissa Heitmann - Hopewell Junction NY, US
  • International Classification:
    C07D 241/08
  • US Classification:
    544385
  • Abstract:
    The disclosed embodiments detail improved methods for the synthesis of diketopiperazines from amino acids. In particular improved methods for the cyclocondensation and purification of N-protected 3,6-(aminoalkyl)-2,5-diketopiperazines from N-protected amino acids. Disclosed embodiments describe methods for the synthesis of 3,6-bis-[N-protected aminoalkyl]-2,5-diketopiperazine comprising heating a mixture of an amino acid in the presence of a catalyst in an organic solvent. The catalyst is selected from the group comprising sulfuric acid, phosphoric acid, p-toluenesulfonic acid, 1-propylphosphonic acid cyclic anhydride, tributyl phosphate, phenyl phosphonic acid and phosphorous pentoxide among others. The solvent is selected from the group comprising: dimethylacetamide, N-methyl-2-pyrrolidone, diglyme, ethyl glyme, proglyme, ethyldiglyme, m-cresol, p-cresol, o-cresol, xylenes, ethylene glycol and phenol among others.
  • Formation Of N-Protected 3,6-Bis-(4-Aminoalkyl)-2,5,Diketopiperazine

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  • US Patent:
    20230034201, Feb 2, 2023
  • Filed:
    Sep 12, 2022
  • Appl. No.:
    17/942576
  • Inventors:
    - Valencia CA, US
    Adrienne Stamper - Naugatuck CT, US
    Melissa Heitmann - Hopewell Junction NY, US
  • International Classification:
    C07D 241/08
    B01J 31/02
  • Abstract:
    The disclosed embodiments detail improved methods for the synthesis of diketopiperazines from amino acids. In particular improved methods for the cyclocondensation and purification of N-protected 3,6-(aminoalkyl)-2,5-diketopiperazines from N-protected amino acids. Disclosed embodiments describe methods for the synthesis of 3,6-bis-[N-protected aminoalkyl]-2,5-diketopiperazine comprising heating a mixture of an amino acid in the presence of a catalyst in an organic solvent. The catalyst is selected from the group comprising sulfuric acid, phosphoric acid, p-toluenesulfonic acid, 1-propylphosphonic acid cyclic anhydride, tributyl phosphate, phenyl phosphonic acid and phosphorous pentoxide among others. The solvent is selected from the group comprising: dimethylacetamide, N-methyl-2-pyrrolidone, diglyme, ethyl glyme, proglyme, ethyldiglyme, m-cresol, p-cresol, o-cresol, xylenes, ethylene glycol and phenol among others.
  • Formation Of N-Protected 3,6-Bis-(4-Aminoalkyl)-2,5,Diketopiperazine

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  • US Patent:
    20200262797, Aug 20, 2020
  • Filed:
    May 4, 2020
  • Appl. No.:
    16/866056
  • Inventors:
    - Valencia CA, US
    Adrienne Stamper - Naugatuck CT, US
    Melissa Heitmann - Hopewell Junction NY, US
  • International Classification:
    C07D 241/08
    B01J 31/02
  • Abstract:
    The disclosed embodiments detail improved methods for the synthesis of diketopiperazines from amino acids. In particular improved methods for the cyclocondensation and purification of N-protected 3,6-(aminoalkyl)-2,5-diketopiperazines from N-protected amino acids. Disclosed embodiments describe methods for the synthesis of 3,6-bis-[N-protected aminoalkyl]-2,5-diketopiperazine comprising heating a mixture of an amino acid in the presence of a catalyst in an organic solvent. The catalyst is selected from the group comprising sulfuric acid, phosphoric acid, p-toluenesulfonic acid, 1-propylphosphonic acid cyclic anhydride, tributyl phosphate, phenyl phosphonic acid and phosphorous pentoxide among others. The solvent is selected from the group comprising: dimethylacetamide, N-methyl-2-pyrrolidone, diglyme, ethyl glyme, proglyme, ethyldiglyme, m-cresol, p-cresol, o-cresol, xylenes, ethylene glycol and phenol among others.
  • Formation Of N-Protected 3,6-Bis-(4-Aminoalkyl)-2,5,Diketopiperazine

    view source
  • US Patent:
    20190169135, Jun 6, 2019
  • Filed:
    Feb 4, 2019
  • Appl. No.:
    16/266683
  • Inventors:
    - Valencia CA, US
    Adrienne Stamper - Naugatuck CT, US
    Melissa Heitmann - Hopewell Junction NY, US
  • International Classification:
    C07D 241/08
    B01J 31/02
  • Abstract:
    The disclosed embodiments detail improved methods for the synthesis of diketopiperazines from amino acids. In particular improved methods for the cyclocondensation and purification of N-protected 3,6-(aminoalkyl)-2,5-diketopiperazines from N-protected amino acids. Disclosed embodiments describe methods for the synthesis of 3,6-bis-[N-protected am inoalkyl]-2,5-diketopiperazine comprising heating a mixture of an amino acid in the presence of a catalyst in an organic solvent. The catalyst is selected from the group comprising sulfuric acid, phosphoric acid, p-toluenesulfonic acid, 1-propylphosphonic acid cyclic anhydride, tributyl phosphate, phenyl phosphonic acid and phosphorous pentoxide among others. The solvent is selected from the group comprising: dimethylacetamide, N-methyl-2-pyrrolidone, diglyme, ethyl glyme, proglyme, ethyldiglyme, m-cresol, p-cresol, o-cresol, xylenes, ethylene glycol and phenol among others.
  • Formation Of N-Protected Bis-3,6-(4-Aminoalkyl)-2,5,Diketopiperazine

    view source
  • US Patent:
    20160347721, Dec 1, 2016
  • Filed:
    Aug 15, 2016
  • Appl. No.:
    15/237427
  • Inventors:
    - Valencia CA, US
    Adrienne Stamper - Naugatuck CT, US
    Melissa Heitmann - Hopewell Junction NY, US
  • International Classification:
    C07D 241/08
  • Abstract:
    The disclosed embodiments detail improved methods for the synthesis of diketopiperazines from amino acids. In particular improved methods for the cyclocondensation and purification of N-protected 3,6-(aminoalkyl)-2,5-diketopiperazines from N-protected amino acids. Disclosed embodiments describe methods for the synthesis of 3,6-bis-[N-protected aminoalkyl]-2,5-diketopiperazine comprising heating a mixture of an amino acid in the presence of a catalyst in an organic solvent. The catalyst is selected from the group comprising sulfuric acid, phosphoric acid, p-toluenesulfonic acid, 1-propylphosphonic acid cyclic anhydride, tributyl phosphate, phenyl phosphonic acid and phosphorous pentoxide among others. The solvent is selected from the group comprising: dimethylacetamide, N-methyl-2-pyrrolidone, diglyme, ethyl glyme, proglyme, ethyldiglyme, m-cresol, p-cresol, o-cresol, xylenes, ethylene glycol and phenol among others.
  • Formation Of N-Protected Bis-3,6-(4-Aminoalkyl)-2,5,Diketopiperazine

    view source
  • US Patent:
    20150073149, Mar 12, 2015
  • Filed:
    Nov 17, 2014
  • Appl. No.:
    14/543464
  • Inventors:
    - Valencia CA, US
    Adrienne Stamper - Naugatuck CT, US
    Melissa Heitmann - Hopewell Junction NY, US
  • International Classification:
    C07D 241/08
  • US Classification:
    544385
  • Abstract:
    The disclosed embodiments detail improved methods for the synthesis of diketopiperazines from amino acids. In particular improved methods for the cyclocondensation and purification of N-protected 3,6-(aminoalkyl)-2,5-diketopiperazines from N-protected amino acids. Disclosed embodiments describe methods for the synthesis of 3,6-bis-[N-protected aminoalkyl]-2,5-diketopiperazine comprising heating a mixture of an amino acid in the presence of a catalyst in an organic solvent. The catalyst is selected from the group comprising sulfuric acid, phosphoric acid, p-toluenesulfonic acid, 1-propylphosphonic acid cyclic anhydride, tributyl phosphate, phenyl phosphonic acid and phosphorous pentoxide among others. The solvent is selected from the group comprising: dimethylacetamide, N-methyl-2-pyrrolidone, diglyme, ethyl glyme, proglyme, ethyldiglyme, m-cresol, p-cresol, o-cresol, xylenes, ethylene glycol and phenol among others.

Resumes

Melissa Heitmann Photo 1

Process Engineer

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Location:
Hopewell Junction, NY
Industry:
Pharmaceuticals
Work:
Mannkind Corporation
Process Engineer

Hudson Highlands Veterinary Medical Group 2003 - 2007
Veterinary Assistant

Proton Onsite 2001 - 2003
Chemical Engineer
Education:
Rensselaer Polytechnic Institute 1997 - 2001
Bachelors, Bachelor of Science, Chemical Engineering

Plaxo

Melissa Heitmann Photo 2

Melissa Heitmann

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Myspace

Melissa Heitmann Photo 3

Melissa Heitmann

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Locality:
SALEM
Gender:
Female
Birthday:
1939

Youtube

Dr Melissa Heightman - Long COVID: recovery o...

Dr Melissa Heightman - Long COVID: recovery on hold!

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    33m 20s

I won't gymnastics

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March 11, 2022

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    8s

He pranks his mom pretending to crack his bac...

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My real name is Victoria

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Hehehe

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    1m 13s

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Melissa Heitmann

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Melissa Heitmann

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Melissa Carmean Heitmann

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Melissa Heitmann

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Melissa Heitmann

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