Pyridine → HCID 23122059, compound

HRID 312838Notes

Reaction equation

HRID 312838 reaction equation
[CH:39]([Cl:40])([Cl:41])[Cl:42].[c:1]1([C:7]2([c:17]3[cH:18][cH:19][cH:20][cH:21][cH:22]3)[O:8][C:9](=[O:16])[N:10]3[CH:11]2[CH2:12][NH:13][CH2:14][CH2:15]3)[cH:2][cH:3][cH:4][cH:5][cH:6]1.[c:29]1([S:35](=[O:36])(=[O:37])[Cl:38])[cH:30][cH:31][cH:32][cH:33][cH:34]1.[cH:23]1[cH:24][cH:25][n:26][cH:27][cH:28]1>>[c:1]1([C:7]2([c:17]3[cH:18][cH:19][cH:20][cH:21][cH:22]3)[O:8][C:9](=[O:16])[N:10]3[CH:11]2[CH2:12][N:13]([S:35]([c:29]2[cH:30][cH:31][cH:32][cH:33][cH:34]2)(=[O:36])=[O:37])[CH2:14][CH2:15]3)[cH:2][cH:3][cH:4][cH:5][cH:6]1

Participants

5

Reactant 4

HCID 1049PyridineHCID 6212ChloroformHCID 7369Benzenesulfonyl chlorideHCID 231218811,1-Diphenyltetrahydro-1H-oxazolo[3,4-a]pyrazin-3(5H)-one

Product 1

HCID 23122059HCID 23122059, compound

Sources & evidence

ORD record
ord-5bfa704a6cb142d8a12336a5699b002a
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction notes

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