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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206390Generated: November 3, 2026

Trifluoroacetic acid → HCID 72201100, compound

https://huagongshe.com/reaction/2206390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 72550900HCID 72550900—
SolventDichloromethaneHCID 6344—
ProductHCID 72201100HCID 7220110090%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of chiral 2-(di-tert-butoxyphosphoryloxy)ethyl 4-((2R,3S,4R,5S)-3-(3-chloro-2-fluorophenyl)-4-(4-chloro-2-fluorophenyl)-4-cyano-5-neopentylpyrrolidine-2-carboxamido)-3-methoxybenzoate (Example 12, 89.1 mg, 0.104 mmol) in methylene chloride (2 mL) was treated with trifluoroacetic acid (1 mL) and stirred for 45 min at 0° C. The reaction mixture was concentrated and the product was lyophilized to give chiral 2-(phosphonooxy)ethyl 4-((2R,3S,4R,5S)-3-(3-chloro-2-fluorophenyl)-4-(4-chloro-2-fluorophenyl)-4-cyano-5-neopentylpyrrolidine-2-carboxamido)-3-methoxybenzoate trifluoroacetate as a white solid (80.7 mg, 90% yield). MS (ES+) m/z calcd. for C33H35Cl2F2N3O8P: [(M+H)+]: 740. found: 740.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371280B2
Source datasetuspto-grants-2016_06
ORD IDord-2ca50640a7104b809d215d724ff116f5
Source noteuspto-grants-2016_06