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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2367350생성일: 2026년 10월 27일

Triethylamine → N-(2-oxo-2-phenylethyl)-4-(phenylmethyl)-2-morpholinecarboxamide

https://huagongshe.com/reaction/2367350

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물PhenacylamineHCID 11952—
반응물Oxalyl chlorideHCID 65578—
반응물4-Benzylmorpholine-2-carboxylic acidHCID 2776353—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물N-(2-oxo-2-phenylethyl)-4-(phenylmethyl)-2-morpholinecarboxamideHCID 6699071132.7%

반응 조건

온도25 °C

반응 단계

Oxalyl chloride (1.187 mL, 13.56 mmol) was added to a suspension of 4-(phenylmethyl)-2-morpholinecarboxylic acid (2.0 g, 9.04 mmol) in CH2Cl2 (70 mL) at 0° C. in 10 minutes, and the resulting mixture was stirred at 25° C. for 2 hours. The mixture was concentrated, and the resulting residue was treated with CH2Cl2 (70 mL), triethylamine (2.77 mL, 19.89 mmol) and 2-amino-1-phenylethanone (1.551 g, 9.04 mmol) at 0° C. The reaction mixture was stirred at 25° C. for 3 hours. Water (150 mL) was added, and the resulting aqueous mixture was extracted with EtOAc (3×80 mL). The combined organic layers were dried (Na2SO4), filtered, and concentrated. The resulting residue was purified by silica gel chromatography to afford the title compound (1.0 g) as a brown solid. LC-MS (ES) m/z=339 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08697685B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-9ecaec64a047446cb929100dcddea6ba
출처 메모uspto-grants-2014_04