반응 #439894

ord-405f23a9a18b419d81bad8c3a3c52499

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

The title compound was prepared with conventional EDC coupling of 3-[2-methyl-(1S)-1-(naphthalene-2-carbonyl-amino)-propyl]-5-phenoxymethyl-4,5-dihydro-isoxazole-5-carboxylic acid (1.00 g, 2.24 mmol) and (3S)-3-amino-4-hydroxy-5-phenoxy-pentanoic acid t-butyl ester (630 mg, 1.0 eq), EDC (558 mg, 1.3 eq), HOBt (394 mg, 1.3 eq) and triethylamine (0.94 mL, 3.0 eq) in DMF (5 mL). Usual workup followed by flash chromatography gave 1.44 g of coupled product. The coupled product and Dess-Martin reagent (2.15 g, 2.5 mol eq) in dry CH2Cl2 (25 mL) under N2 at room temperature was stirred for 1 h, then quenched with isopropyl alcohol (3 mL). Usual extractive workup followed by flash chromatography (36% ethyl acetate-hexane) gave 1.27 g of the tide compound as diastereomeric mixture. Preparative HPLC (36% ethyl acetate-hexanes, 10 mL/min, 278 nm UV detection) afforded less polar (352 mg) and more polar (536 mg) diastereomers.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06747050B1uspto-grants-2004_06