Hydrogen Bromide → 3-Bromo-5-chloro-N-(7-methoxy-4,5-dihydronaphtho[1,2-d][1,3]thiazol-2-yl)-2-thiophenesulfonamide

HRID 2336421Notes

Reaction equation

HRID 2336421 reaction equation
[Br:18][c:19]1[c:20]([S:25](=[O:26])(=[O:27])[Cl:28])[s:21][c:22]([Cl:24])[cH:23]1.[BrH:1].[CH3:2][O:3][c:4]1[cH:5][c:6]2[c:15]([cH:16][cH:17]1)-[c:10]1[c:9]([s:13][c:12]([NH2:14])[n:11]1)[CH2:8][CH2:7]2>>[CH3:2][O:3][c:4]1[cH:5][c:6]2[c:15]([cH:16][cH:17]1)-[c:10]1[c:9]([s:13][c:12]([NH:14][S:25]([c:20]3[c:19]([Br:18])[cH:23][c:22]([Cl:24])[s:21]3)(=[O:26])=[O:27])[n:11]1)[CH2:8][CH2:7]2

Participants

4

Reactant 3

HCID 260Hydrogen BromideHCID 6906227-Methoxy-4,5-dihydronaphtho[1,2-d]thiazol-2-amineHCID 27374003-Bromo-5-chlorothiophene-2-sulfonyl chloride

Product 1

HCID 101635393-Bromo-5-chloro-N-(7-methoxy-4,5-dihydronaphtho[1,2-d][1,3]thiazol-2-yl)-2-thiophenesulfonamide

Sources & evidence

ORD record
ord-74c5a87af8f04802a2c2da8c10e349fd
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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