Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037455Generated: October 31, 2026

HCID 66857138, compound → HCID 58109164, compound

https://huagongshe.com/reaction/2037455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66857138HCID 66857138—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
ProductHCID 58109164HCID 5810916461.1%

Reaction Steps

A solution of tert-butyl 2-(2-((R)-3-((S)-1-(2′,4′-difluorobiphenyl-4-yl)ethyl)-6-(4-fluorophenyl)-2-oxo-1,3-oxazinan-6-yl)ethylamino)-2-oxoethylcarbamate (98 mg, 0.16 mmol) in TFA/CH2Cl2 (20%, 5 mL) was stirred at 0° C. for 2 h. The solvent was evaporated to give the crude product, which was purified by preparative HPLC to afford 2-amino-N-(2-((R)-3-((S)-1-(2′,4′-difluorobiphenyl-4-yl)ethyl)-6-(4-fluorophenyl)-2-oxo-1,3-oxazinan-6-yl)ethyl)acetamide (50 mg, 60%). 1H NMR (CDCl3): 1.41-1.49 (d, 3H), 2.15-2.29 (m, 5H), 2.80-2.94 (m, 2H), 3.25-3.36 (m, 1H), 3.70-3.85 (m, 2H), 5.50 (m, 1H), 6.75-6.97 (m, 7H), 7.00-7.14 (m, 3H), 7.26-7.29 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575156B2
Source datasetuspto-grants-2013_11
ORD IDord-d18da0e9f9044ea4930e9f58977358a7
Source noteuspto-grants-2013_11