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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071937Generated: October 27, 2026

4-amino-N-(2-methoxyethyl)benzene-1-sulfonamide → HCID 10110828, compound

https://huagongshe.com/reaction/1071937

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-amino-N-(2-methoxyethyl)benzene-1-sulfonamideHCID 16781918—
ReactantHCID 22390594HCID 22390594—
Solvent(+-)-2-ButanolHCID 6568—
ProductHCID 10110828HCID 1011082877.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

2-Chloro-5-cyano-4-cyclopropylaminopyrimidine (Method 96; 295 mg, 1.28 mmol) was dissolved in hot 2-butanol (3 ml). A hot solution of 4-[N-(2-methoxyethyl)sulphamoyl]aniline (Method 5; 207 mg, 0.90 mmol) in 2-butanol (3 ml) was added and the reaction was stirred and heated at 90° C. for 1 hour. The reaction mixture was cooled and the volatiles evaporated to give a solid. The solid residue was triturated with hot ethyl acetate, cooled, and the resultant solid collected by filtration to give the title compound (270 mg, 77%). NMR: 0.68 (m, 2H), 0.80 (m, 2H), 2.88 (m, 3H), 3.14 (s, 3H), 3.28 (m, 2H), 7.48 (brs, 1H), 7.70 (d, 2H), 8.05 (d, 2H), 8.12 (brs, 1H) 8.41 (s, 1H), 10.31 (s, 1H); m/z: 389.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06908920B2
Source datasetuspto-grants-2005_06
ORD IDord-66a55060a6414b15985b012386beee66
Source noteuspto-grants-2005_06