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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037533Generated: October 30, 2026

Ammonia → HCID 58109425, compound

https://huagongshe.com/reaction/2037533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantHCID 53361128HCID 53361128—
SolventDichloromethaneHCID 6344—
ProductHCID 58109425HCID 5810942535%

Reaction Steps

(S)-3-((S)-1-(2′,4′-difluorobiphenyl-4-yl)ethyl)-6-(4-fluorophenyl)-6-(2-hydroxyethyl)-1,3-oxazinan-2-one (50 mg, 0.11 mmol) was dissolved in CH2Cl2 (3 mL), followed by the addition of TEA (1 mL) and 4-nitrophenyl carbonochloridate (88 mg, 0.44 mmol). The mixture was stirred at rt overnight. Aqueous ammonia (2 mL) was added and the mixture was stirred at rt for 3 h. After separation of the water layer, the organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo to give the crude product, which was purified by preparative TLC to afford 2-((S)-3-((S)-1-(2′,4′-difluorobiphenyl-4-yl)ethyl)-6-(4-fluorophenyl)-2-oxo-1,3-oxazinan-6-yl)ethyl carbamate (20 mg, 35%). LC-MS Method 3 tR=1.36, min, m/z=499; 1H NMR (CDCl3): 1.48 (m, 3H), 2.14-2.33 (m, 5H), 2.91 (m, 1H), 3.42 (s, 1H), 3.95 (m, 1H), 4.07 (m, 1H), 4.62 (s, 2H), 5.61 (m, 1H), 6.79-7.01 (m, 6H), 7.23 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575156B2
Source datasetuspto-grants-2013_11
ORD IDord-963c0d976b854e4ea8f867d4cbfbd9ca
Source noteuspto-grants-2013_11