Cis tert-Butyl 4-aminocyclohexylcarbamate → HCID 66866732, compound

HRID 2146989Notes

Reaction equation

HRID 2146989 reaction equation
[C:26]([CH3:27])([CH3:28])([CH3:29])[O:30][C:31]([NH:32][CH:33]1[CH2:34][CH2:35][CH:36]([NH2:39])[CH2:37][CH2:38]1)=[O:40].[CH3:1][O:2][c:3]1[cH:4][c:5]([O:21][CH2:22][CH2:23][O:24][CH3:25])[c:6](-[c:9]2[c:10]3[c:11]([n:12][cH:13][n:14]2)[c:15]([C:18](=[O:19])[OH:20])[cH:16][nH:17]3)[cH:7][cH:8]1>>[CH3:1][O:2][c:3]1[cH:4][c:5]([O:21][CH2:22][CH2:23][O:24][CH3:25])[c:6](-[c:9]2[c:10]3[c:11]([n:12][cH:13][n:14]2)[c:15]([C:18](=[O:20])[NH:39][CH:36]2[CH2:35][CH2:34][CH:33]([NH:32][C:31]([O:30][C:26]([CH3:27])([CH3:28])[CH3:29])=[O:40])[CH2:38][CH2:37]2)[cH:16][nH:17]3)[cH:7][cH:8]1

Participants

3

Reactant 2

HCID 2756050Cis tert-Butyl 4-aminocyclohexylcarbamateHCID 66866942HCID 66866942, compound

Product 1

HCID 66866732HCID 66866732, compound

Sources & evidence

ORD record
ord-a2a4eae519dd440b8d533b5d8111e043
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

Loading…