Hydrazine, 1,1-diphenyl-, hydrochloride (1:1) → HCID 22049495, compound

HRID 2087599Notes

Reaction equation

HRID 2087599 reaction equation
O1CCO[CH:2]1[CH2:6][CH2:7][CH2:8][N:9]1[CH2:14][CH2:13][CH:12]([C:15]2[CH:16]=[C:17]([NH:21][C:22](=[O:26])[CH:23]([CH3:25])[CH3:24])[CH:18]=[CH:19][CH:20]=2)[CH2:11][CH2:10]1.Cl.[C:28]1([N:34]([C:36]2[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=2)N)[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>>[CH3:25][CH:23]([CH3:24])[C:22]([NH:21][C:17]1[CH:18]=[CH:19][CH:20]=[C:15]([CH:12]2[CH2:13][CH2:14][N:9]([CH2:8][CH2:7][C:6]3[C:29]4[C:28](=[CH:33][CH:32]=[CH:31][CH:30]=4)[N:34]([C:36]4[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=4)[CH:2]=3)[CH2:10][CH2:11]2)[CH:16]=1)=[O:26]

Participants

3

Reactant 2

HCID 10738Hydrazine, 1,1-diphenyl-, hydrochloride (1:1)HCID 22048812HCID 22048812, compound

Product 1

HCID 22049495HCID 22049495, compound

Procedure

Prepared by Procedure H and Scheme S using N-(3-{1-[3-(1,3-dioxolan-2-yl)propyl]-4-piperidinyl}phenyl)-2-methylpropanamide and 1,1-diphenylhydrazine hydrochloride: ESMS m/e: 466.2 (M+H)+.

Workup

  1. customPrepared by Procedure H and Scheme S

Sources & evidence

ORD record
ord-0d21769c88e24bbc91dfe8b0e39897db
Source dataset
uspto-grants-2004_04
Patent number
US06727264B1

Reaction notes

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