Dichloromethane → N-(4-methyl-5-{5-[(prop-2-yn-1-ylamino)sulfonyl]-2-thienyl}-1,3-thiazol-2-yl)acetamide

HRID 2347736Notes

Reaction equation

[C:1]([CH3:2])(=[O:3])[NH:4][c:5]1[s:6][c:7](-[c:11]2[cH:12][cH:13][c:14]([S:16](=[O:17])(=[O:18])[Cl:19])[s:15]2)[c:8]([CH3:10])[n:9]1.[CH2:20]([C:21]#[CH:22])[NH2:23].[CH:24]([N:25]([CH:26]([CH3:27])[CH3:28])[CH2:29][CH3:30])([CH3:31])[CH3:32].[Cl:33][CH2:34][Cl:35]>>[C:1]([CH3:2])(=[O:3])[NH:4][c:5]1[s:6][c:7](-[c:11]2[cH:12][cH:13][c:14]([S:16](=[O:17])(=[O:18])[NH:23][CH2:20][C:21]#[CH:22])[s:15]2)[c:8]([CH3:10])[n:9]1

Participants

Reactant 4

HCID 6344Dichloromethane

HCID 81531Diisopropylethylamine

HCID 239041Propargylamine

HCID 866225625-[2-(Acetylamino)-4-methyl-1,3-thiazol-5-yl]thiophene-2-sulfonyl chloride

Product 1

HCID 11998301N-(4-methyl-5-{5-[(prop-2-yn-1-ylamino)sulfonyl]-2-thienyl}-1,3-thiazol-2-yl)acetamide

Sources & evidence

ORD record: ord-19546e0764164934b8ee61963e230bcf
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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