Vincent A Pavia, Age 92468 Leedsville Rd, Amenia, NY 12501

Vincent Pavia Phones & Addresses

468 Leedsville Rd, Amenia, NY 12501

Norton, MA

53 Holly Hill Dr, Wingdale, NY 12594

Croton on Hudson, NY

Lagrangeville, NY

Port Chester, NY

Wappingers Falls, NY

Wappingers Fl, NY

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Work

Position: Sales Occupations

Education

Degree: Associate degree or higher

Mentions for Vincent A Pavia

Vincent Pavia resumes & CV records

Resumes

Vincent Pavia Photo 20

Senior Chemical Operator

Location:
468 Leedsville Rd, Amenia, NY 12501
Industry:
Pharmaceuticals
Work:
Mannkind Corporation
Senior Chemical Operator
Skills:
Biotechnology, Quality Control
Vincent Pavia Photo 21

Vincent Pavia

Publications & IP owners

Us Patents

Methods For The Synthesis Of Activated Ethylfumarates And Their Use As Intermediates

US Patent:
2021011, Apr 22, 2021
Filed:
Dec 7, 2020
Appl. No.:
17/113540
Inventors:
- Westlake Village CA, US
John J. Freeman - New Fairfield CT, US
Paul Serwinski - Bristol CT, US
Vincent Pavia - Valencia CA, US
Otto Phanstiel - Oviedo FL, US
Navneet Kaur - Danbury CT, US
International Classification:
C07D 241/08
C07C 201/12
C07C 67/39
C07C 67/30
Abstract:
Disclosed embodiments relate to improved methods for the synthesis of activated fumarate intermediates and their use in chemical synthesis. Disclosed embodiments describe the synthesis of activated fumarate esters including those derived from activating groups including: 4-nitrophenyl, diphenylphophoryl azide, pivaloyl chloride, chlorosulfonyl isocyanate, p-nitrophenol, MEF, trifluoroacetyl and chlorine, for example, ethyl fumaroyl chloride and the subsequent use of the activated ester in situ. Further embodiments describe the improved synthesis of substituted aminoalkyl-diketopiperazines from unisolated and unpurified intermediates allowing for improved yields and reactor throughput.

Methods For The Synthesis Of Activated Ethylfumarates And Their Use As Intermediates

US Patent:
2019001, Jan 10, 2019
Filed:
Sep 10, 2018
Appl. No.:
16/126323
Inventors:
- Westlake Village CA, US
John J. Freeman - New Fairfield CT, US
Paul Serwinski - Bristol CT, US
Vincent Pavia - Valencia CA, US
Otto Phanstiel - Oviedo FL, US
Navneet Kaur - Danbury CT, US
International Classification:
C07D 241/08
C07C 201/12
C07C 67/30
C07C 67/39
C07C 69/60
C07C 205/43
Abstract:
Disclosed embodiments relate to improved methods for the synthesis of activated fumarate intermediates and their use in chemical synthesis. Disclosed embodiments describe the synthesis of activated fumarate esters including those derived from activating groups including: 4-nitrophenyl, diphenylphophoryl azide, pivaloyl chloride, chlorosulfonyl isocyanate, p-nitrophenol, MEF, trifluoroacetyl and chlorine, for example, ethyl fumaroyl chloride and the subsequent use of the activated ester in situ. Further embodiments describe the improved synthesis of substituted aminoalkyl-diketopiperazines from unisolated and unpurified intermediates allowing for improved yields and reactor throughput.

Methods For The Synthesis Of Activated Ethylfumarates And Their Use As Intermediates

US Patent:
2016015, Jun 9, 2016
Filed:
Nov 23, 2015
Appl. No.:
14/949489
Inventors:
- Valencia CA, US
John J. Freeman - New Fairfield CT, US
Paul Serwinski - Bristol CT, US
Vincent Pavia - Valencia CA, US
Otto Phansteil - Oviedo FL, US
Navneet Kaur - Danbury CT, US
International Classification:
C07D 241/08
Abstract:
Disclosed embodiments relate to improved methods for the synthesis of activated fumarate intermediates and their use in chemical synthesis. Disclosed embodiments describe the synthesis of activated fumarate esters including those derived from activating groups including: 4-nitrophenyl, diphenylphophoryl azide, pivaloyl chloride, chlorosulfonyl isocyanate, p-nitrophenol, MEF, trifluoroacetyl and chlorine, for example, ethyl fumaroyl chloride and the subsequent use of the activated ester in situ. Further embodiments describe the improved synthesis of substituted aminoalkyl-diketopiperazines from unisolated and unpurified intermediates allowing for improved yields and reactor throughput.

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