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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1823018생성일: 2026년 10월 25일

Triethylamine → (R)-1-[4-(3-Fluoro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acid methylamide

https://huagongshe.com/reaction/1823018

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
반응물Methylamine hydrochlorideHCID 6364545—
반응물(S)-1-[4-(3-fluoro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acidHCID 67409315—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물(R)-1-[4-(3-Fluoro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acid methylamideHCID 10020247—

반응 단계

A solution of 0.339 g (1.03 mmol) of (S)-1-[4-(3-fluoro-benzyloxy)-phenyl]-5-oxo-pyrrolidine-3-carboxylic acid in 21 ml of N,N-dimethylformamide, cooled to 0° C., is treated consecutively with 0.15 ml (1.13 mmol) of triethylamine, 0.390 g (1.03 mmol) of HBTU, 0.085 g (1.24 mmol) of methylamine hydrochloride, and 0.15 ml (1.13 mmol) of triethylamine. The reaction is stopped after 30 min and the orange colored solution is evaporated under reduced pressure. The residue obtained is triturated in ethyl acetate, the white solid product is filtered, thereafter dissolved in dichloromethane and the solution washed three times with water. The organic phase is dried over sodium sulfate, then evaporated under reduced pressure to yield 231 mg (66% of theory) of a white solid. MS: m/e=343 (M+H)+; [α]589=−25.48° (c=0.954, CH2Cl2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07037935B2
출처 데이터셋uspto-grants-2006_05
ORD IDord-33cba6c66bf8469ebdfda023b09d112d
출처 메모uspto-grants-2006_05