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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782641Generated: October 30, 2026

Hydrochloric Acid → HCID 68818026, compound

https://huagongshe.com/reaction/1782641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 68819599HCID 68819599—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68818026HCID 68818026—

Reaction Steps

2N Sodium hydroxide solution (1.32 mL, 2.64 mmol) was added dropwise to a stirred solution of (2R)-methyl-2-tert-butoxycarbonylamino-3-(4′-dibenzofuran-4-yl-biphenyl-4-ylmethylsulfanyl)propionate (500 mg, 0.88 mmol) in tetrahydrofuran (15 mL) and methanol (3 mL). The clear reaction mixture was stirred at room temperature until the reaction was complete (TLC control), and then diluted with water (10 mL), and acidified to pH 3 with 2N hydrochloric acid. The reaction mixture was extracted with ethyl acetate (2×20 mL). The combined extract was washed with water, brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo. Purification of the product by flash column chromatography, using 5-10% methanol in methylene chloride as eluent, afforded the title compound has a white solid (420 mg, 87%), m.pt. 205-206° C.; Rf: 0.40 (10% methanol in dichloromethane); 1H NMR (MeOH-d4): δ 7.90 (4H, m, Ar—H), 7.67 (2H, d, J=9 Hz, Ar—H), 7.56 (2H, d, J=9 Hz, Ar—H), 7.53 (2H, d, J=8 Hz, Ar—H), 7.29-7.41 (5H, m, Ar—H), 4.34 (1H, m, CHN), 3.87 (2H, s, PhCH2S), 2.95 (1H, dd, J=15, 5 Hz, CHHCHN), 2.86 (1H, dd, J=15, 7 Hz, CHHCHN), 1.42 (9H, s, CMe3); ESI-LCMS e/z calcd for C33H31NO5S 553.676, found 554 (M+H)+, 576 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498356B2
Source datasetuspto-grants-2009_03
ORD IDord-db804fd692aa4260a1641b4997e4a7cb
Source noteuspto-grants-2009_03