Acetonitrile → tert-butyl 6-amino-7-iodo-1-methyl-1H-imidazo[4,5-c]pyridin-4-yl(2,4-dimethoxybenzyl)carbamate

反応式

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

参加物

反応物 3

HCID 6342Acetonitrile

HCID 120273N-Iodosuccinimide

HCID 58180570Tert-butyl 2,4-dimethoxybenzyl6-amino-1-methyl-1h-imidazo[4,5-c]pyridin-4-ylcarbamate

生成物 1

HCID 58180507tert-butyl 6-amino-7-iodo-1-methyl-1H-imidazo[4,5-c]pyridin-4-yl(2,4-dimethoxybenzyl)carbamate

出典と根拠

ORDレコード: ord-def383715fca483aa32834ec50ed733e
出典データセット: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D

反応ノート

読み込み中…