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1-Methyl-2-oxopiperidine-4-carboxylic acid → HCID 86674654, compound

HRID 245709
Notes
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Reaction equation

HRID 245709 reaction equation
Cl.[NH2:2][CH2:3][C:4]1[C:9]([Cl:10])=[N:8][CH:7]=[CH:6][N:5]=1.[CH3:11][N:12]1[CH2:17][CH2:16][CH:15]([C:18](O)=[O:19])[CH2:14][C:13]1=[O:21]>>[Cl:10][C:9]1[C:4]([CH2:3][NH:2][C:18]([CH:15]2[CH2:16][CH2:17][N:12]([CH3:11])[C:13](=[O:21])[CH2:14]2)=[O:19])=[N:5][CH:6]=[CH:7][N:8]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 222654461-Methyl-2-oxopiperidine-4-carboxylic acidHCID 42614233(3-Chloropyrazin-2-yl)methanamine hydrochloride

Product 1

HCID 86674654HCID 86674654, compoundYield 62%

Procedure

2-Aminomethyl-3-chloropyrazine hydrochloride (content 77%; 5.36 mmol, 1.0 g) and 1-methyl-2-oxopiperidine-4-carboxylic acid (5.36 mmol, 0.843 g) were applied according to the procedure in example 13 step 13a and purified using column chromatography (silica gel; dichloromethane with 10% methanol) to give N-((3-chloropyrazin-2-yl)methyl)-1-methyl-2-oxopiperidine-4-carboxamide (940 mg).

Workup

  1. custompurified

Sources & evidence

ORD record
ord-253886c950ab4ce69832388fef5e53af
Source dataset
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08658794B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes