Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29368Generated: October 29, 2026

Diisopropylethylamine → (S)-3-methyl-2-{4'-[(3-methyl-4-pyridin-4-yl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid methyl ester

https://huagongshe.com/reaction/29368

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 methyl esterHCID 59847687—
Reactant3-Methyl-4-pyridin-4-yl-benzofuran-2-carboxylic acidHCID 68715081—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
Product(S)-3-methyl-2-{4'-[(3-methyl-4-pyridin-4-yl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid methyl esterHCID 6871532182.2%

Reaction Steps

To 3-methyl-4-pyridin-4-yl-benzofuran-2-carboxylic acid (88 mg, 0.35 mmol) in 4 mL of DMF was added (S)-2-(4′-amino-biphenyl-4-sulfonylamino)-3-methyl-butyric acid methyl ester (252 mg, 0.7 mmol), BOP (307 mg, 0.7 mmol), and N,N-diisopropylethylamine (0.12 mL, 0.7 mmol). 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 the solvent in vacuo gave the crude product, which was purified by column chromatography on silica gel to give 172 mg of (S)-3-methyl-2-{4′-[(3-methyl-4-pyridin-4-yl-benzofuran-2-carbonyl)-amino]-biphenyl-4-sulfonylamino}-butyric acid methyl ester, obtained as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420001B2
Source datasetuspto-grants-2008_09
ORD IDord-2f35960436314c388cc85b3542ff0be9
Source noteuspto-grants-2008_09