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Ammonia → HCID 117966096, compound

HRID 56225
Notes
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Reaction equation

HRID 56225 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([NH:23][C:24](=[O:29])[CH2:25][C:26](=O)[CH3:27])[CH:5]=[CH:6][C:7]=1[NH:8][C:9]([CH3:22])([CH3:21])[CH2:10][C:11]1[CH:20]=[CH:19][C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:12]=1.[NH3:30]>CO>[NH2:30]/[C:26](/[CH3:27])=[CH:25]\[C:24]([NH:23][C:4]1[CH:5]=[CH:6][C:7]([NH:8][C:9]([CH3:21])([CH3:22])[CH2:10][C:11]2[CH:20]=[CH:19][C:18]3[C:17](=[CH:16][CH:15]=[CH:14][CH:13]=3)[CH:12]=2)=[C:2]([Cl:1])[CH:3]=1)=[O:29]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 222AmmoniaHCID 90023565N-(3-chloro-4-((2-methyl-1-(naphthalen-2-yl)propan-2-yl)amino)phenyl)-3-oxobutanamide

Product 1

HCID 117966096HCID 117966096, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

A mixture of N-(3-chloro-4-((2-methyl-1-(naphthalen-2-yl)propan-2-yl)amino) phenyl)-3-oxobutanamide (2.0 g, 4.89 mmol), MeOH (15 mL) and ammonia (15 mL) was stirred at rt overnight. The mixture was then concentrated in vacuo to give the title compound, which was used for next step without further purification.

Workup

  1. concentrationThe mixture was then concentrated in vacuo

Sources & evidence

ORD record
ord-31187eba04b6454cb5397242bcda0f3e
Source dataset
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09434695B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes