Cyclooctylamine → HCID 21101801, compound

HRID 1118628Notes

Reaction equation

HRID 1118628 reaction equation
[CH:1]1([NH2:9])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]1.[CH:23]([N:24]([CH:25]([CH3:26])[CH3:27])[CH2:28][CH3:29])([CH3:30])[CH3:31].[Cl:10][C:11](=[O:12])[O:13][c:14]1[cH:15][cH:16][c:17]([N+:18]([O-:19])=[O:20])[cH:21][cH:22]1.[Cl:32][c:33]1[cH:34][cH:35][c:36]2[c:37]([N:43]3[CH2:44][CH2:45][NH:46][CH2:47][CH2:48]3)[cH:38][cH:39][n:40][c:41]2[cH:42]1>>[CH:1]1([NH:9][C:11](=[O:12])[N:46]2[CH2:45][CH2:44][N:43]([c:37]3[c:36]4[cH:35][cH:34][c:33]([Cl:32])[cH:42][c:41]4[n:40][cH:39][cH:38]3)[CH2:48][CH2:47]2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]1

Participants

5

Reactant 4

HCID 2903CyclooctylamineHCID 81531DiisopropylethylamineHCID 821294-Nitrophenyl chloroformateHCID 7383897-Chloro-4-(piperazin-1-yl)quinoline

Product 1

HCID 21101801HCID 21101801, compound

Sources & evidence

ORD record
ord-6e4e99bb65644585ad45e832453b3dcd
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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