2-(1H-pyrazol-1-yl)ethanamine → HCID 59605497, compound

HRID 1923134Notes

Reaction equation

HRID 1923134 reaction equation
[CH3:1][N:2]1[C:10]([CH:11]=O)=[N:9][C:8]2[C:3]1=[N:4][C:5]([N:19]1[C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=3[N:21]=[C:20]1[CH3:28])=[N:6][C:7]=2[N:13]1[CH2:18][CH2:17][O:16][CH2:15][CH2:14]1.[N:29]1([CH2:34][CH2:35][NH2:36])[CH:33]=[CH:32][CH:31]=[N:30]1>>[CH3:1][N:2]1[C:10]([CH2:11][NH:36][CH2:35][CH2:34][N:29]2[CH:33]=[CH:32][CH:31]=[N:30]2)=[N:9][C:8]2[C:3]1=[N:4][C:5]([N:19]1[C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=3[N:21]=[C:20]1[CH3:28])=[N:6][C:7]=2[N:13]1[CH2:14][CH2:15][O:16][CH2:17][CH2:18]1

Participants

3

Procedure

Following General Procedure L for reductive amination, 9-methyl-2-(2-methyl-1H-benzo[d]imidazol-1-yl)-6-morpholino-9H-purine-8-carbaldehyde and 2-(1H-pyrazol-1-yl)ethanamine were reacted to give 431. [M+H]+ 473.3

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-dc275db053494269ac8f1b5c166186e5
Source dataset
uspto-grants-2012_05
Patent number
US08173650B2

Reaction notes

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