Pyridine → HCID 44526983, compound

HRID 1122921Notes

Reaction equation

HRID 1122921 reaction equation
[CH2:34]1[CH2:35][CH2:36][NH:37][CH2:38][CH2:39]1.[Cl:46][S:47]([OH:48])(=[O:49])=[O:50].[NH2:1][c:2]1[n:3][cH:4][c:5](-[c:12]2[cH:13][c:14]3[c:15](-[c:22]4[cH:23][cH:24][n:25][cH:26][cH:27]4)[cH:16][cH:17][n:18][c:19]3[cH:20][cH:21]2)[cH:6][c:7]1[S:8](=[O:9])(=[O:10])[Cl:11].[O:28]1[CH2:29][CH2:30][O:31][CH2:32][CH2:33]1.[cH:40]1[cH:41][cH:42][n:43][cH:44][cH:45]1>>[NH2:1][c:2]1[n:3][cH:4][c:5](-[c:12]2[cH:13][c:14]3[c:15](-[c:22]4[cH:23][cH:24][n:25][cH:26][cH:27]4)[cH:16][cH:17][n:18][c:19]3[cH:20][cH:21]2)[cH:6][c:7]1[S:8](=[O:9])(=[O:10])[N:37]1[CH2:36][CH2:35][CH2:34][CH2:39][CH2:38]1

Participants

6

Reactant 5

HCID 1049PyridineHCID 8082PiperidineHCID 24638Chlorosulfonic acidHCID 312751,4-DioxaneHCID 86625113HCID 86625113, compound

Product 1

HCID 44526983HCID 44526983, compound

Sources & evidence

ORD record
ord-35c8d721bf9d416a93a1740dcb05447c
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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