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Ammonia → HCID 59578441, compound

HRID 1897829
Notes
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Reaction equation

HRID 1897829 reaction equation
C[O:2][C:3](=O)[CH2:4][CH2:5][C:6]1[CH:7]=[N:8][CH:9]=[C:10]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([Cl:18])[C:13]=2[Cl:19])[CH:11]=1.[NH3:21]>>[Cl:19][C:13]1[C:14]([Cl:18])=[CH:15][CH:16]=[CH:17][C:12]=1[C:10]1[CH:11]=[C:6]([CH2:5][CH2:4][C:3]([NH2:21])=[O:2])[CH:7]=[N:8][CH:9]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 222Ammonia2×HCID 595784053-[5-(2,3-Dichloro-phenyl)-pyridin-3-yl]-propionic acid methyl ester

Product 1

HCID 59578441HCID 59578441, compound

Procedure

A mixture of 3-[5-(2,3-dichloro-phenyl)-pyridin-3-yl]-propionic acid methyl ester and ammonia (7N in MeOH, 2 ml, 14.00 mmol) was stirred at room temperature for 24 hours. Ammonia (7N in MeOH, 1 ml, 7.00 mmol) was added, and the reaction mixture was stirred for another 24 hours. Solvent was removed in vacuo. The crude product was used in the next step without purification. ESI-MS m/z: 295 [M+1]+.

Workup

  1. stirringthe reaction mixture was stirred for another 24 hours
  2. customSolvent was removed in vacuo
  3. customThe crude product was used in the next step without purification
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Sources & evidence

ORD record
ord-a3fc54d7c3904939a4e591ac30b719b2
Source dataset
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08519142B2

Reaction notes

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