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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771248Generated: October 25, 2026

(R)-Benzyl (2,5-dioxotetrahydrofuran-3-yl)carbamate → HCID 88578517, compound

https://huagongshe.com/reaction/1771248

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-Benzyl (2,5-dioxotetrahydrofuran-3-yl)carbamateHCID 12416472—
ReactantDi-tert-butyl ((R)-(4'-chlorobiphenyl-2-yl)(1-(4-(4-((R)-4-morpholino-1-(phenylthio)butan-2-ylamino)-3-(trifluoromethylsulfonyl)phenylsulfonylcarbamoyl)-phenyl)piperidin-4-yl)methoxy)methyl phosphateHCID 131734652—
SolventAcetoneHCID 180—
ProductHCID 88578517HCID 8857851730.3%

Reaction Conditions

Temperature65 °C

Reaction Steps

Nitrolotrimethanol (5.27 mg, 0.05 mmol) was added to a solution of di-tert-butyl ((R)-(4′-chlorobiphenyl-2-yl)(1-(4-(4-((R)-4-morpholino-1-(phenylthio)butan-2-ylamino)-3-(trifluoromethylsulfonyl)phenylsulfonylcarbamoyl)phenyl)piperidin-4-yl)methoxy)methyl phosphate (EXAMPLE 27, 58.0 mg, 0.05 mmol) in acetone (1.8 ml) and 0.6 ml of pH7.2 buffer (Gibco, Dulbecco's Phosphate Buffered saline 1×). The resulting reaction mixture was stirred at 65° C. for 16 hours. Evaporation of the volatiles under reduced pressure gave a residue which was purified by reverse phase HPLC (Gilson column, eluting with 30→50% H2O with 10 mM NH4OAc/MeCN for 5 minutes) to provide the title product (0.017 g, yield: 19%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248140B2
Source datasetuspto-grants-2016_02
ORD IDord-97612f8274f046aca759c27574b72d83
Source noteuspto-grants-2016_02