Neopentylamine → HCID 58656493, compound

HRID 1988947Notes

Reaction equation

HRID 1988947 reaction equation
[CH:1]1([NH:4][C:5]([C:7]2[CH:8]=[CH:9][C:10]([CH3:27])=[C:11]([C:13]3[CH:14]=[C:15]4[C:19](=[CH:20][CH:21]=3)[N:18]([CH2:22][C:23](OC)=[O:24])[N:17]=[CH:16]4)[CH:12]=2)=[O:6])[CH2:3][CH2:2]1.[CH3:28][C:29]([CH3:33])([CH3:32])[CH2:30][NH2:31]>>[CH:1]1([NH:4][C:5](=[O:6])[C:7]2[CH:8]=[CH:9][C:10]([CH3:27])=[C:11]([C:13]3[CH:14]=[C:15]4[C:19](=[CH:20][CH:21]=3)[N:18]([CH2:22][C:23]([NH:31][CH2:30][C:29]([CH3:33])([CH3:32])[CH3:28])=[O:24])[N:17]=[CH:16]4)[CH:12]=2)[CH2:3][CH2:2]1

Participants

3

Reactant 2

HCID 79882NeopentylamineHCID 58656497HCID 58656497, compound

Product 1

HCID 58656493HCID 58656493, compound

Procedure

Example 130 was prepared by General Method D using methyl (5-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-1H-indazol-1-yl)acetate (Example 117) and 2,2-dimethyl-1-propanamine to give the title compound (0.015 g).

Workup

  1. customExample 130 was prepared by General Method D

Sources & evidence

ORD record
ord-e073f5a6b0354ab5b8798936a7c8619b
Source dataset
uspto-grants-2010_01
Patent number
US07642276B2

Reaction notes

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