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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78949Generated: October 26, 2026

Ammonia → 2-[(R)-(Carbamoylphenylmethyl)-amino]-3-(4-methoxyphenyl)-2-(S)-methylpropionamide

https://huagongshe.com/reaction/78949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSulfuric AcidHCID 1118—
ReactantDichloromethaneHCID 6344—
Reactant(R)-2-(((S)-2-cyano-1-(4-methoxyphenyl)propan-2-yl) amino)-2-phenylacetamideHCID 67200502—
SolventEthyl AcetateHCID 8857—
Product2-[(R)-(Carbamoylphenylmethyl)-amino]-3-(4-methoxyphenyl)-2-(S)-methylpropionamideHCID 67167012—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a 500 mL flask were added nitrile 2 (10.0 g, 30.95 mmol) and CH2Cl2 (130 mL). The solution was cooled to −10° C. and H2SO4 (10 mL) was added dropwise over 15 min. The mixture was stirred for 2 h at 0° C. Ice (200 g) was added and the mixture was stirred for 1 h. The mixture was basified with 32% aq NH3 to pH 8-9, EtOAc (400 mL) was added and the phases were separated. The aqueous phase was extracted with EtOAc (2×250 mL). The combined organic phases were dried over MgSO4 and were concentrated to provide 3 (11.1 g (9.99 g theoretical, the sample contains 10% w/w of EtOAc by NMR) 94%, 92.9% chemical purity, 97% de by HPLC/MS) as a white solid. HPLC/MS tR=3.04 min; m/z=342.1 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841486B2
Source datasetuspto-grants-2014_09
ORD IDord-5b7042aa79594fc7986d5d8042e1dca5
Source noteuspto-grants-2014_09