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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785049Generated: October 28, 2026

Trifluoroacetic acid → HCID 67278023, compound

https://huagongshe.com/reaction/1785049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropylamineHCID 7912—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 57594128HCID 57594128—
Reactant1,1-dimethylethyl (4R)-4-(([(1,1-dimethylethyl)oxy]carbonyl}amino)-5-[4-(8-methylimidazo[1,2-a]pyridin-2-yl)phenyl]pentanoateHCID 67278371—
SolventDichloromethaneHCID 6344—
ProductHCID 67278023HCID 6727802361%

Reaction Steps

To a solution of 1,1-dimethylethyl (4R)-4-(([(1,1-dimethylethyl)oxy]carbonyl}amino)-5-[4-(8-methylimidazo[1,2-a]pyridin-2-yl)phenyl]pentanoate (1.35 g, 2.82 mmol) in CH2Cl2 (14 mL) was added trifluoroacetic acid (10 mL) followed by triethylsilane (2.5 equiv, 7.04 mmol). The reaction was stirred for 45 minutes at room temperature and then concentrated in vacuo. DMF (35 mL) was added to the residue followed by diisopropylamine (14.7 mL, 84.51 mmol) under nitrogen. The reaction was stirred for 5 minutes and pentafluorophenyl 3-chloro-4-[(1-methylethyl)oxy]benzoate (1.1 equiv, 3.10 mmol) was added. The reaction was stirred for 45 minutes and then concentrated in vacuo. Ethyl acetate (50 mL) was added to the residue and it was washed with H2O (30 mL). The aqueous layer was extracted with EtOAc (20 mL) and the combined organic layers were dried over MgSO4 and concentrated in vacuo. Purification by silica gel chromatography (Analogix IF280, 25-100% EtOAc/hexanes) provided the title compound as a white foamy solid (61%). ESMS [M+H]+=520.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504413B2
Source datasetuspto-grants-2009_03
ORD IDord-d72ee98388eb46d4be26dc716f355c6d
Source noteuspto-grants-2009_03