Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865757Generated: October 30, 2026

Water → HCID 11317482, compound

https://huagongshe.com/reaction/1865757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantHCID 86596613HCID 86596613—
ReactantHCID 86596614HCID 86596614—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11317482HCID 11317482—

Reaction Conditions

Temperature60 °C

Reaction Steps

According to General Procedure II, a 1:1 mixture of ethyl (E,4S)-4-[((2S)-2-{[(2S)-2-methoxy-3-methyl-3-phenylbutanoyl]amino}-3,3-dimethylbutanoyl)(methyl)amino]-2,5-dimethyl-2-hexenoate and ethyl (E,4S)-4-[((2S)-2-{[(2R)-2-methoxy-3-methyl-3-phenylbutanoyl]amino}-3,3-dimethylbutanoyl)(methyl)amino]-2,5-dimethyl-2-hexenoate (1.0 g, 2.0 mmol, from Reference Example 104) is dissolved in methanol (10 mL) and tetrahydrofuran (10 mL). To this solution is added water (5 mL) and lithium hydroxide monohydrate (0.17 g, 4.0 mmol), and the resulting mixture is stirred at 60° C. for 16 hours. Solvents are removed in vacuo and the residue is then dissolved in water. The solution is acidified to pH 1 with 2 M aqueous hydrochloric acid solution and then extracted thrice with ethyl acetate. The combined extracts are washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, decanted, and concentrated under reduced pressure to afford a white foam. A sample of this crude material (240 mg) is subjected to HPLC purification (Prodigy OS3 column, acetonitrile/water/TFA) to give (E,4S)-4-[{N-[(2S)-2-methoxy-3-methyl-3-phenylbutanoyl]-3-methyl-L-valyl}(methyl)amino]-2,5-dimethyl-2-hexenoic acid as a hard white foam (50 mg). MS (ES+): (M+H)=475.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07626023B2
Source datasetuspto-grants-2009_12
ORD IDord-4932906016a848c7b2c50e4201c31ae5
Source noteuspto-grants-2009_12