Hydrochloric Acid → tert-butyl 3-(6-amino-8-oxo-7H-purin-9(8H)-yl)phenylcarbamate

反応式

[CH2:1]([N:8]([CH2:2][c:3]1[cH:4][cH:5][cH:6][cH:7][cH:33]1)[c:9]1[c:10]2[nH:11][c:12](=[O:32])[n:13](-[c:18]3[cH:19][c:20]([NH:24][C:25]([O:26][C:27]([CH3:28])([CH3:29])[CH3:30])=[O:31])[cH:21][cH:22][cH:23]3)[c:14]2[n:15][cH:16][n:17]1)[c:34]1[cH:35][cH:36][cH:37][cH:38][cH:39]1.[CH3:41][OH:42].[ClH:40]>>[NH2:8][c:9]1[c:10]2[nH:11][c:12](=[O:32])[n:13](-[c:18]3[cH:19][c:20]([NH:24][C:25]([O:26][C:27]([CH3:28])([CH3:29])[CH3:30])=[O:31])[cH:21][cH:22][cH:23]3)[c:14]2[n:15][cH:16][n:17]1

参加物

反応物 3

HCID 313Hydrochloric Acid

HCID 887Methanol

HCID 86691210tert-Butyl 3-(6-(dibenzylamino)-8-oxo-7H-purin-9(8H)-yl)phenylcarbamate

生成物 1

HCID 86691212tert-butyl 3-(6-amino-8-oxo-7H-purin-9(8H)-yl)phenylcarbamate

出典と根拠

ORDレコード: ord-a40ab361d5eb4832a7e38f9943112e78
出典データセット: Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI: 10.1039/C8SC04228D

反応ノート

読み込み中…