HRID1545284

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID923

Sodium ion

Na+

HCID28123

Tetrahydroborate

H4B-

HCID12045001

tert-Butyl 4-[(4-aminophenyl)methyl]piperazine-1-carboxylate

C16H25N3O2

结构：CNc1ccc(CN2CCN(C(=O)OC(C)(C)C)C(C)C2)cc1

HCID178482156

未命名化合物

PRODUCTS

生成物

结构：CNc1ccc(CN2CCN(C(=O)OC(C)(C)C)CC2)cc1

HCID46835451

tert-Butyl 4-{[4-(methylamino)phenyl]methyl}piperazine-1-carboxylate

C17H27N3O2

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-ff99444e659143c08cbefb11f9381658
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (1/10)

反应 SMILES

[BH4-:45].[CH3:22][CH:23]1[N:24]([C:38](=[O:39])[O:40][C:41]([CH3:42])([CH3:43])[CH3:44])[CH2:25][CH2:26][N:27]([CH2:29][c:30]2[cH:31][cH:32][c:33]([NH:36][CH3:37])[cH:34][cH:35]2)[CH2:28]1.[NH2:1][c:2]1[cH:3][cH:4][c:5]([CH2:6][N:7]2[CH2:8][CH2:9][N:10]([C:11]([O:12][C:13]([CH3:14])([CH3:15])[CH3:16])=[O:17])[CH2:18][CH2:19]2)[cH:20][cH:21]1.[Na+:46]>>[CH2:23]1[N:24]([C:38](=[O:39])[O:40][C:41]([CH3:42])([CH3:43])[CH3:44])[CH2:25][CH2:26][N:27]([CH2:29][c:30]2[cH:31][cH:32][c:33]([NH:36][CH3:37])[cH:34][cH:35]2)[CH2:28]1