N-Hydroxynicotinimidamide → HCID 58002714, compound

HRID 1642959Notes

Reaction equation

HRID 1642959 reaction equation
[N:1]1([C:7]([N:9]2[CH2:14][CH:13]([C:15]3[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:17][CH:16]=3)[CH2:12][CH:11]([C:25]([OH:27])=O)[CH2:10]2)=[O:8])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.O[N:29]=[C:30]([C:32]1[CH:33]=[N:34][CH:35]=[CH:36][CH:37]=1)[NH2:31]>>[N:34]1[CH:35]=[CH:36][CH:37]=[C:32]([C:30]2[N:31]=[C:25]([CH:11]3[CH2:12][CH:13]([C:15]4[CH:20]=[CH:19][C:18]([C:21]([F:22])([F:23])[F:24])=[CH:17][CH:16]=4)[CH2:14][N:9]([C:7]([N:1]4[CH2:6][CH2:5][O:4][CH2:3][CH2:2]4)=[O:8])[CH2:10]3)[O:27][N:29]=2)[CH:33]=1

Participants

3

Reactant 2

HCID 308113N-HydroxynicotinimidamideHCID 580024471-(Morpholin-4-ylcarbonyl)-5-[4-(trifluoromethyl)phenyl]piperidine-3-carboxylic acid

Product 1

HCID 58002714HCID 58002714, compound

Procedure

250 mg (about 0.65 mmol) of 1-(morpholin-4-ylcarbonyl)-5-[4-(trifluoromethyl)phenyl]piperidine-3-carboxylic acid and 98 mg (0.71 mmol) of N′-hydroxypyridine-3-carboximidamide were reacted according to the General Method 1. Yield: 35 mg (11% of theory)

Sources & evidence

ORD record
ord-a31dd0513b004042bd9bbe1affdc7e77
Source dataset
uspto-grants-2012_02
Patent number
US08119663B2

Reaction notes

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