4-(N-Boc-amino)piperidine → HCID 86608263, 화합물

반응식

[Cl:24][c:25]1[n:26][c:27]([CH2:32][CH2:33][CH2:34][CH3:35])[n:28][c:29]([CH3:31])[cH:30]1.[N+:1]([c:2]1[c:3]([N:10]2[CH2:11][CH2:12][CH:13]([NH:16][C:17]([O:18][C:19]([CH3:20])([CH3:21])[CH3:22])=[O:23])[CH2:14][CH2:15]2)[n:4][cH:5][cH:6][cH:7]1)([O-:8])=[O:9].[NH:36]1[CH2:37][CH2:38][CH:39]([NH:40][C:41](=[O:42])[O:43][C:44]([CH3:45])([CH3:46])[CH3:47])[CH2:48][CH2:49]1>>[N:10]1([c:25]2[n:26][c:27]([CH2:32][CH2:33][CH2:34][CH3:35])[n:28][c:29]([CH3:31])[cH:30]2)[CH2:11][CH2:12][CH:13]([NH:16][C:17]([O:18][C:19]([CH3:20])([CH3:21])[CH3:22])=[O:23])[CH2:14][CH2:15]1

참가 물질

반응물 3

HCID 7238334-(N-Boc-amino)piperidine

HCID 176064082-Butyl-4-chloro-6-methylpyrimidine

HCID 44120582tert-Butyl (1-(3-nitropyridin-2-yl)piperidin-4-yl)carbamate

생성물 1

HCID 86608263HCID 86608263, 화합물

출처 및 근거

ORD 기록: ord-45cb148bc9c24cefab30b907a52dff80
출처 데이터셋: Training data from https://doi.org/10.1039/C8SC04228D (7/10)
DOI: 10.1039/C8SC04228D

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