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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516453Generated: November 3, 2026

Acetone → HCID 86705145, compound

https://huagongshe.com/reaction/516453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantDiethyl EtherHCID 3283—
ReactantTetrahydrofuranHCID 8028—
ReactantBromomethyl acetateHCID 68536—
ReactantHCID 72700307HCID 72700307—
SolventAcetic AcidHCID 176—
SolventPalladiumHCID 23938—
ProductHCID 86705145HCID 8670514534.4%

Reaction Conditions

Temperature45 °C

Reaction Steps

Bromomethyl acetate (6.7 μL, 68.3 μmol) and Et2O (11.7 μL, 84 μmol) were added to a solution of (2R,4R)-4-[(3-benzyloxy-3H-benzotriazole-5-carbonyl)amino]-5-(3′-chlorobiphenyl-4-yl)-2-hydroxypentanoic acid (30.0 mg, 52.5 μmol) in acetone (1.0 mL, 13.6 mmol) and the resulting mixture was stirred at 45° C. for 1 hour. A drop of AcOH was added to neutralize the reaction and the mixture was concentrated to yield a clear yellow liquid. The crude liquid was purified (C18 column chromatography, 55 g column, using 40-90% MeCN in water with 0.05% TFA) to yield a white solid. The solid was dissolved in THF (1.0 mL, 12.3 mmol) and 10% Pd/C, 50% wet (0.45 mmol/g loading; 5.8 mg, 2.6 μmol) was added to the solution, which was stirred under hydrogen for 1 hour. The mixture was filtered and the filtrate was concentrated to yield a clear colorless liquid. The crude liquid was purified (preparative scale C18 column chromatography, small column, using 30-90% MeCN in water with 0.05% TFA) to yield the title compound as a white solid (10.0 mg, purity 99%). MS m/z [M+H]+ calc'd for C27H25ClN4O7, 553.14. found 553.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108934B2
Source datasetuspto-grants-2015_08
ORD IDord-47feac073fb64191ba5bcd1b0a52e894
Source noteuspto-grants-2015_08