5-Bromo-2-ethoxypyridin-3-amine → N-(5-Bromo-2-ethoxypyridin-3-yl)-4-hydroxy-3-methylbenzenesulfonamide

HRID 1052520Notes

Reaction equation

HRID 1052520 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([NH2:11])[C:5]([O:8][CH2:9][CH3:10])=[N:6][CH:7]=1.[OH:12][C:13]1[CH:18]=[CH:17][C:16]([S:19](Cl)(=[O:21])=[O:20])=[CH:15][C:14]=1[CH3:23]>>[Br:1][C:2]1[CH:3]=[C:4]([NH:11][S:19]([C:16]2[CH:17]=[CH:18][C:13]([OH:12])=[C:14]([CH3:23])[CH:15]=2)(=[O:21])=[O:20])[C:5]([O:8][CH2:9][CH3:10])=[N:6][CH:7]=1

Participants

3

Reactant 2

HCID 532116995-Bromo-2-ethoxypyridin-3-amineHCID 552806724-Hydroxy-3-methylbenzene-1-sulfonyl chloride

Product 1

HCID 90103249N-(5-Bromo-2-ethoxypyridin-3-yl)-4-hydroxy-3-methylbenzenesulfonamideYield 100%

Procedure

5-Bromo-2-ethoxypyridin-3-amine (506 mg, 2.33 mmol) was treated with 4-hydroxy-3-methylbenzene-1-sulfonyl chloride (506 mg, 2.45 mmol, prepared as described at JP 47015818 B4 19720511) according to the method described in Preparation 15b to give 902 mg (100% yield) of the title compound as an oil. Purity 99%.

Sources & evidence

ORD record
ord-d0452207c47942778cf9b7ff98711939
Source dataset
uspto-grants-2016_07
Patent number
US09388189B2

Reaction notes

Loading…