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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365505Generated: November 2, 2026

Hydrochloric Acid → HCID 66934465, compound

https://huagongshe.com/reaction/1365505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAnilineHCID 6115—
ReactantPyBroPHCID 2733179—
ReactantHCID 66934634HCID 66934634—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
SolventMethanol--water (1/1)HCID 22242641—
ProductHCID 66934465HCID 6693446558%

Reaction Steps

(S)-3-(5-chloropyridin-2-yl)-3-(3-fluoro-5-(trifluoromethyl)phenyl)-3-pivalamidopropanoic acid (0.10 g, 0.21 mmol) was dissolved in MeOH (2 mL) and 4M HCl in dioxanes added (2 mL). The resulting solution was stirred at RT for 30 mins then the solvents were removed under reduced pressure yielding a pale yellow oil (crude quantative) LCMS: 1.31 min [M+1] 363.2 (2 min gradient, MeOH/H2O 0.1% TFA). The residue was dissolved in acetonitrile (5 mL) and TEA, (0.3 mL, excess), aniline (0.030 g, 0.32 mmol) and PyBrOP (0.11 g, 0.24 mmol) added at RT. The RM was stirred for 14 h, concentrated to 1.5 mL, filtered and purified by prep HPLC: YMC ODSA30×100 mm, 40ml/min, 20-100% MeOH (0.1% TFA) over 10 min. The product (S)-3-amino-3-(5-chloropyridin-2-yl)-3-(3-fluoro-5-(trifluoromethyl)phenyl)-N-phenylpropanamide with a retention time of 7.52 min was isolated as a pale yellow oil, (0.054 g, 58% yield). LCMS: 1.48 min [M+1] 438.2 (2 min gradient, MeOH/H2O 0.1% TFA).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888376B2
Source datasetuspto-grants-2011_02
ORD IDord-6640dede3ac64167ad42dc9fe066e5a9
Source noteuspto-grants-2011_02