4-Fluorobenzenesulfonyl chloride → HCID 23288138, compound

HRID 670900Notes

Reaction equation

HRID 670900 reaction equation
[Cl:28][c:29]1[cH:30][c:31]2[c:32]([c:33]([CH:34]3[CH2:35][CH2:36][N:37]([CH3:38])[CH2:39][CH2:40]3)[cH:41][nH:42]2)[cH:43][cH:44]1.[F:1][c:2]1[cH:3][cH:4][c:5]([S:8](=[O:9])(=[O:10])[n:11]2[cH:12][c:13]([CH:21]3[CH2:22][CH2:23][N:24]([CH3:27])[CH2:25][CH2:26]3)[c:14]3[cH:15][cH:16][c:17]([Cl:20])[cH:18][c:19]23)[cH:6][cH:7]1.[F:45][c:46]1[cH:47][cH:48][c:49]([S:50]([Cl:51])(=[O:52])=[O:53])[cH:54][cH:55]1>>[cH:2]1[cH:3][cH:4][c:5]([S:8](=[O:9])(=[O:10])[n:11]2[cH:12][c:13]([CH:21]3[CH2:22][CH2:23][N:24]([CH3:27])[CH2:25][CH2:26]3)[c:14]3[cH:15][cH:16][c:17]([Cl:20])[cH:18][c:19]23)[cH:6][cH:7]1

Participants

4

Reactant 3

HCID 95884-Fluorobenzenesulfonyl chlorideHCID 187973681H-Indole, 6-chloro-3-(1-methyl-4-piperidinyl)-HCID 23288102HCID 23288102, compound

Product 1

HCID 23288138HCID 23288138, compound

Sources & evidence

ORD record
ord-ca9c9ff4efda4fb58edf5e1c0da405cf
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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