Tetrahydrofuran → 2-(4-Aminophenyl)-3-[4-(2-(1-pyrrolidinyl)ethoxy]benzyl]benzo[b]thiophene

반응식

[C:33]([O-:34])(=[O:35])[C:36]([O-:37])=[O:38].[CH2:39]1[O:40][CH2:41][CH2:42][CH2:43]1.[N:1]1([CH2:6][CH2:7][O:8][c:9]2[cH:10][cH:11][c:12]([C:15](=[O:16])[c:17]3[c:18]4[c:19]([s:20][c:21]3-[c:22]3[cH:23][cH:24][c:25]([NH2:28])[cH:26][cH:27]3)[cH:29][cH:30][cH:31][cH:32]4)[cH:13][cH:14]2)[CH2:2][CH2:3][CH2:4][CH2:5]1>>[N:1]1([CH2:6][CH2:7][O:8][c:9]2[cH:10][cH:11][c:12]([CH2:15][c:17]3[c:18]4[c:19]([s:20][c:21]3-[c:22]3[cH:23][cH:24][c:25]([NH2:28])[cH:26][cH:27]3)[cH:29][cH:30][cH:31][cH:32]4)[cH:13][cH:14]2)[CH2:2][CH2:3][CH2:4][CH2:5]1

참가 물질

반응물 3

HCID 8028Tetrahydrofuran

HCID 71081Oxalate

HCID 224627242-(4-Aminophenyl)benzo[b]thiophene-3-yl 4-[2-(1-pyrrolidinyl)ethoxy]phenyl ketone

생성물 1

HCID 224627922-(4-Aminophenyl)-3-[4-(2-(1-pyrrolidinyl)ethoxy]benzyl]benzo[b]thiophene

출처 및 근거

ORD 기록: ord-452696b9aa3544b89d03b1065c132bb8
출처 데이터셋: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D

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