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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884451Generated: October 26, 2026

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

https://huagongshe.com/reaction/884451

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-ylbenzoic 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 numberUS08242115B2
Source datasetuspto-grants-2012_08
ORD IDord-3decffbd6e1b4b29ac3696896c9a025a
Source noteuspto-grants-2012_08