Dichloromethane → N-(5-methoxypyridin-3-yl)-3-(2-methyl-9H-purin-6-yl)pyridin-2-amine

反応式

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

参加物

反応物 3

HCID 6344Dichloromethane

HCID 6422Trifluoroacetic acid

HCID 66600712N-(5-methoxypyridin-3-yl)-3-(2-methyl-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl)pyridin-2-amine

生成物 1

HCID 178493745N-(5-methoxypyridin-3-yl)-3-(2-methyl-9H-purin-6-yl)pyridin-2-amine

出典と根拠

ORDレコード: ord-eca4f149f71548c2a141a62a51211469
出典データセット: Training data from https://doi.org/10.1039/C8SC04228D (7/10)
DOI: 10.1039/C8SC04228D

反応ノート

読み込み中…