Dimethyl Sulfoxide → HCID 20192943, compound

HRID 2315236Notes

Reaction equation

HRID 2315236 reaction equation
[C:18](=[O:19])([O-:20])[O-:21].[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[s:6][c:7]2[c:8]([n:9]1)[cH:10][c:11]([Cl:17])[c:12]([N+:14](=[O:15])[O-:16])[cH:13]2.[CH3:24][CH:25]1[CH2:26][NH:27][CH2:28][CH2:29][CH2:30]1.[CH3:32][S:33](=[O:34])[CH3:35].[CH:36]([Cl:37])([Cl:38])[Cl:39].[K+:22].[K+:23].[OH2:31]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[c:5]1[s:6][c:7]2[c:8]([n:9]1)[cH:10][c:11]([N:27]1[CH2:26][CH:25]([CH3:24])[CH2:30][CH2:29][CH2:28]1)[c:12]([N+:14](=[O:15])[O-:16])[cH:13]2

Participants

8

Reactant 7

HCID 679Dimethyl SulfoxideHCID 813Potassium Cation2×HCID 962WaterHCID 6212ChloroformHCID 19660Carbonate IonHCID 790813-MethylpiperidineHCID 197942022-Tert-butyl-5-chloro-6-nitrobenzothiazole

Product 1

HCID 20192943HCID 20192943, compound

Sources & evidence

ORD record
ord-239ee01929544190b50ac300975a1c0d
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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