Cycloheptylamine → HCID 21101679, compound

HRID 699571Notes

Reaction equation

HRID 699571 reaction equation
[CH:1]1([NH2:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]1.[CH:22]([N:23]([CH:24]([CH3:25])[CH3:26])[CH2:27][CH3:28])([CH3:29])[CH3:30].[Cl:31][c:32]1[cH:33][cH:34][c:35]2[c:36]([N:43]3[CH2:44][CH2:45][NH:46][CH2:47][CH2:48]3)[cH:37][c:38]([NH2:42])[n:39][c:40]2[cH:41]1.[Cl:9][C:10](=[O:11])[O:12][c:13]1[cH:14][cH:15][c:16]([N+:17]([O-:18])=[O:19])[cH:20][cH:21]1>>[CH:1]1([NH:8][C:10](=[O:11])[N:46]2[CH2:45][CH2:44][N:43]([c:36]3[c:35]4[cH:34][cH:33][c:32]([Cl:31])[cH:41][c:40]4[n:39][c:38]([NH2:42])[cH:37]3)[CH2:48][CH2:47]2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]1

Participants

5

Reactant 4

HCID 2899CycloheptylamineHCID 81531DiisopropylethylamineHCID 821294-Nitrophenyl chloroformateHCID 211017487-Chloro-4-(1-piperazinyl)-2-quinolinamine

Product 1

HCID 21101679HCID 21101679, compound

Sources & evidence

ORD record
ord-9c96f15a1e1445109b0f87eab7a994b4
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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