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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29450Generated: October 30, 2026

Dimethylformamide → (S)-3-methyl-2-{4'-[(5-trifluoromethyl-benzothiazole-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid tert-butyl ester

https://huagongshe.com/reaction/29450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant(S)-2-(4'-amino-biphenyl-4-sulfonylamino)-3-methyl-butyric acid tert-butyl esterHCID 10525284—
Reactant5-Trifluoromethyl-benzothiazole-2-carboxylic acid sodium saltHCID 68713922—
SolventSodium chloride; waterHCID 57417360—
Product(S)-3-methyl-2-{4'-[(5-trifluoromethyl-benzothiazole-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid tert-butyl esterHCID 6871472937.4%

Reaction Steps

To 5-trifluoromethyl-benzothiazole-2-carboxylic acid sodium salt (260 mg, 0.97 mmol) was added (S)-2-(4′-amino-biphenyl-4-sulfonylamino)-3-methyl-butyric acid tert-butyl ester (469 mg, 1.2 eq), BOP (515 mg, 1.2 eq) and 5 mL of DMF. The mixture was stirred at room temperature overnight. The reaction mixture was poured into brine, and extracted with ethyl acetate. The combined organic layers were washed with brine and water. Removal of solvent gave the crude product, which was purified by column chromatography on silica gel to give 230 mg of (S)-3-methyl-2-{4′-[(5-trifluoromethyl-benzothiazole-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid tert-butyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-a8de0e0a6e7a45f6aadfad65a8312bc2
Source noteuspto-grants-2008_09