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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349701Generated: October 27, 2026

Triethylamine → 2-Methylsulfonylamino-4-morpholin-4-yl-benzoic acid

https://huagongshe.com/reaction/349701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN-methyl-N-(trimethylsilyl)trifluoroacetamideHCID 32510—
Reactant2-Amino-4-(morpholin-4-yl)benzoic acidHCID 17808204—
SolventDichloromethaneHCID 6344—
Product2-Methylsulfonylamino-4-morpholin-4-yl-benzoic acidHCID 58805202—

Reaction Steps

To a suspension of 2-amino-4-morpholin-4-yl-benzoic acid (230 mg; 1.04 mmol) in CH2Cl2 (3 mL) was added N-methyl-N-(trimethylsilyl)trifluoroacetamide (0.4 mL; 2.1 mmol) via syringe at room temperature under a nitrogen atmosphere. The resulting mixture was heated to reflux for 10 minutes, then allowed to cool to room temperature. Methanesulfonyl chloride (1.2 eq.) and triethylamine (1.2 eq.) were added, and the resulting mixture allowed to stir for 2 hours. The reaction was diluted with CH2Cl2 (30 mL) and washed with water (2×10 mL) and brine, then dried (MgSO4), filtered, and concentrated in vacuo to provide the sulfonamide as a white solid (280 mg; 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179912B2
Source datasetuspto-grants-2007_02
ORD IDord-eba7adbb842e452f8b50fd0f0a59d6b7
Source noteuspto-grants-2007_02