1-Phenyl-5-propyl-1H-pyrazole-4-carbonyl chloride → HCID 22048694, compound

HRID 2087789Notes

Reaction equation

HRID 2087789 reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][N:8]1[CH2:13][CH2:12][CH:11]([C:14]2[CH:15]=[C:16]([NH:20][C:21](=[O:25])[CH:22]([CH3:24])[CH3:23])[CH:17]=[CH:18][CH:19]=2)[CH2:10][CH2:9]1.[C:26]1([N:32]2[C:36]([CH2:37][CH2:38][CH3:39])=[C:35]([C:40](Cl)=[O:41])[CH:34]=[N:33]2)[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>C1COCC1>[C:21]([NH:20][C:16]1[CH:15]=[C:14]([CH:11]2[CH2:12][CH2:13][N:8]([CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][NH:1][C:40]([C:35]3[CH:34]=[N:33][N:32]([C:26]4[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=4)[C:36]=3[CH2:37][CH2:38][CH3:39])=[O:41])[CH2:9][CH2:10]2)[CH:19]=[CH:18][CH:17]=1)(=[O:25])[CH:22]([CH3:23])[CH3:24]

Participants

4

Reactant 2

HCID 37757171-Phenyl-5-propyl-1H-pyrazole-4-carbonyl chlorideHCID 16755868N-{3-[1-(6-Aminohexyl)4-piperidinyl]phenyl}-2-methylpropanamide

Product 1

HCID 22048694HCID 22048694, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Prepared by Procedure Q1 (THF) and Scheme AT using N-{3-[1-(6-aminohexyl)-4-piperidinyl]phenyl}-2-methylpropanamide and 1-phenyl-5-propyl-1H-pyrazole-4-carbonyl chloride: ESMS m/e: 558.3 (M+H)+.

Sources & evidence

ORD record
ord-9e0a2c2213ee4f7389db178b2160bcab
Source dataset
uspto-grants-2004_04
Patent number
US06727264B1

Reaction notes

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