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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881818Generated: November 1, 2026

Trifluoroacetic acid → HCID 68422702, compound

https://huagongshe.com/reaction/881818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-(4-Methoxy-benzyl)-2H-tetrazole-5-carbonyl chlorideHCID 59607732—
Reactant(R)-ethyl 3-amino-4-(3'-chlorobiphenyl-4-yl)butanoate hydrochlorideHCID 86648190—
SolventDichloromethaneHCID 6344—
ProductHCID 68422702HCID 68422702—

Reaction Steps

To a solution of intermediate 8-1 in DCM (8 ml) at room temperature is added 2-(4-methoxy-benzyl)-2H-tetrazole-5-carbonyl chloride and followed by TEA (Intermediate 22: 0.293 ml, 2.100 mmol). The reaction is stirred at room temperature for 5 min. The reaction is quenched by brine and is extracted with DCM. The combined organic layer is washed with brine and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue is purified by column chromatography (15% to 40% EtOAc/Heptane). The obtained residue in TFA (5 ml, 64.9 mmol) is heated at 80° C. for 0.5 hours. The reaction is concentrated under reduced pressure to give (R)-4-(3′-chloro-biphenyl-4-yl)-3-[(2H-tetrazole-5-carbonyl)-amino]-butyric acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993631B2
Source datasetuspto-grants-2015_03
ORD IDord-386bfd0e87bd42fbac3257ace83b0289
Source noteuspto-grants-2015_03