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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1908141생성일: 2026년 10월 24일

Triethylamine → Spiro[benzo[b]pyrrolo[1,2-d][1,4]oxazine-4,4'-piperidine]-1'-yl(4-(2,2,2-trifluoroethoxy)phenyl)methanone

https://huagongshe.com/ko/reaction/1908141

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-(2,2,2-Trifluoroethoxy)benzoic acidHCID 3763901—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물Spiro[benzo[b]pyrrolo[1,2-d][1,4]oxazine-4,4'-piperidine]HCID 58550727—
용매DimethylformamideHCID 6228—
생성물Spiro[benzo[b]pyrrolo[1,2-d][1,4]oxazine-4,4'-piperidine]-1'-yl(4-(2,2,2-trifluoroethoxy)phenyl)methanoneHCID 58551056—

반응 단계

4-(2,2,2-Trifluoroethoxy)benzoic acid (22 mg, 0.10 mmol), HATU (42 mg, 0.11 mmol), and DMF (0.8 mL) were combined and allowed to sit at room temperature for 10 minutes. The activated acid was then added to spiro[benzo[b]pyrrolo[1,2-d][1,4]oxazine-4,4′-piperidine] (28 mg, 0.10 mmol) followed by the addition of Et3N (84 μL, 0.60 mmol). The reaction mixture was stirred at room temperature for 17 h before it was filtered and purified by prep-HPLC (5 mM HCl/H2O and MeOH) to provide spiro[benzo[b]pyrrolo[1,2-d][1,4]oxazine-4,4′-piperidine]-1′-yl(4-(2,2,2-trifluoroethoxy)phenyl)methanone. ESI-MS m/z calc. 442.2. found 443.4 (M+1)+. Retention time: 2.05 minutes (4 min run).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08598164B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-98e437e7ca52402f83beac9e25f373ea
출처 메모uspto-grants-2013_12