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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265482Generated: October 30, 2026

Hydrochloric Acid → HCID 10161498, compound

https://huagongshe.com/reaction/1265482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant2-AminobenzoxazoleHCID 20707—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant3-Cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-propionic acidHCID 12010541—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 10161498HCID 1016149819.5%

Reaction Steps

A solution of 3-cyclopentyl-2-(4-methanesulfonyl-3-nitrophenyl)-propionic acid (prepared as in Example 32, 50 mg, 0.15 mmol), triethylamine (0.060 mL, 0.44 mmol), benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (98 mg, 0.22 mmol), and 2-aminobenzoxazole (30 mg, 0.22 mmol) in N,N-dimethylformamide (3 mL) was stirred at 25° C. for 3 h. The reaction mixture was then diluted with water (25 mL), a 1N aqueous hydrochloric acid solution (5 mL), and ethyl acetate (25 mL). The layers were separated. The resulting organic layer was washed with a saturated aqueous sodium chloride solution (1×25 mL), dried over magnesium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 2/1 hexanes/ethyl acetate) afforded N-benzooxazol-2-yl-3-cyclopentyl-2-(4-methanesulfonyl-3-nitro-phenyl)-propionamide (13 mg, 19.5%) as a yellow solid: mp 106-110° C.; EI-HRMS m/e calcd for C22H23N3O6S (M+) 457.1308, found 457.1323.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06545155B2
Source datasetuspto-grants-2003_04
ORD IDord-1943411d668e4618a02fc8510d631e4a
Source noteuspto-grants-2003_04