3-tert-butyl-1-phenyl-1H-pyrazol-5-amine → HCID 67021637, compound

HRID 1661001Notes

Reaction equation

HRID 1661001 reaction equation
[N:1]1[C:9]2[C:4](=[N:5][CH:6]=[CH:7][CH:8]=2)[N:3]([C:10]2[CH:15]=[CH:14][C:13]([CH2:16][C:17]([OH:19])=O)=[CH:12][CH:11]=2)[CH:2]=1.[C:20]([C:24]1[CH:25]=[C:26]([NH2:35])[N:27]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[N:28]=1)([CH3:23])([CH3:22])[CH3:21]>>[C:20]([C:24]1[CH:25]=[C:26]([NH:35][C:17](=[O:19])[CH2:16][C:13]2[CH:12]=[CH:11][C:10]([N:3]3[C:4]4=[N:5][CH:6]=[CH:7][CH:8]=[C:9]4[N:1]=[CH:2]3)=[CH:15][CH:14]=2)[N:27]([C:29]2[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=2)[N:28]=1)([CH3:23])([CH3:21])[CH3:22]

Participants

3

Reactant 2

HCID 7706343-tert-butyl-1-phenyl-1H-pyrazol-5-amineHCID 53213084(4-Imidazo[4,5-b]pyridin-3-yl-phenyl)-acetic acid

Product 1

HCID 67021637HCID 67021637, compound

Procedure

The title compound is prepared as described in Example 28 but using 2-(4-imidazo[4,5-b]pyridine-3-yl-phenyl)-acetic acid and 5-tert-butyl-2-phenyl-2H-pyrazol-3-ylamine. Title compound: ES-MS: 451.55 [M+H]+; tR=1.55 min (System 3).

Workup

  1. customThe title compound is prepared

Sources & evidence

ORD record
ord-ae33a6e1b5094a288af767c13244eab0
Source dataset
uspto-grants-2011_10
Patent number
US08030311B2

Reaction notes

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