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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29442Generated: October 29, 2026

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

https://huagongshe.com/reaction/29442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
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-Methyl-benzooxazole-2-carboxylic acid sodium saltHCID 68713096—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product(S)-3-methyl-2-{4'-[(5-methyl-benzooxazole-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid tert-butyl esterHCID 6871104312.8%

Reaction Steps

To 5-methyl-benzooxazole-2-carboxylic acid sodium salt (130 mg, 0.83 mmol) was added (S)-2-(4′-amino-biphenyl-4-sulfonylamino)-3-methyl-butyric acid tert-butyl ester (400 mg, 1.2 eq), BOP (430 mg, 1.2 eq), N,N-diisopropylethylamine (126 mg, 1.2 eq) and 4 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 solution was washed with brine and water. Removal of solvent gave the crude product, which was purified by column chromatography on silica gel to give 60 mg of (S)-3-methyl-2-{4′-[(5-methyl-benzooxazole-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid tert-butyl ester was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-55eb72e3f98748e8b0c0be42e5f01ed2
Source noteuspto-grants-2008_09