2-(Pyridin-3-ylmethyl)isoindoline-1,3-dione → Chloride

反応式

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

参加物

反応物 2

HCID 7094552-(Pyridin-3-ylmethyl)isoindoline-1,3-dione

HCID 1133536310-methoxymethyl-8-chloromethyl-10H-pyrazino[2,3-b][1,4]benzothiazine

生成物 2

HCID 312Chloride

HCID 186702372-[[1-[[10-(Methoxymethyl)pyrazino[2,3-b][1,4]benzothiazin-8-yl]methyl]pyridin-1-ium-3-yl]methyl]isoindole-1,3-dione

出典と根拠

ORDレコード: ord-21f2d4449ab64cb589efde879021fd4c
出典データセット: Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI: 10.1039/C8SC04228D

反応ノート

読み込み中…