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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 390167생성일: 2026년 10월 25일

Methyl iodide → (E)-methyl 1-methyl-2-oxo-1'-(3-(2-(trifluoromethyl)phenyl)acryloyl)spiro[indoline-3,4'-piperidine]-5-carboxylate

https://huagongshe.com/reaction/390167

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물(E)-methyl 2-oxo-1'-(3-(2-(trifluoromethyl)phenyl)acryloyl)spiro[indoline-3,4'-piperidine]-5-carboxylateHCID 58295691—
용매TetrahydrofuranHCID 8028—
생성물(E)-methyl 1-methyl-2-oxo-1'-(3-(2-(trifluoromethyl)phenyl)acryloyl)spiro[indoline-3,4'-piperidine]-5-carboxylateHCID 4422687158%

반응 단계

A solution of (E)-methyl 2-oxo-1′-(3-(2-(trifluoromethyl)phenyl)acryloyl)spiro[indoline-3,4′-piperidine]-5-carboxylate (150 mg, 0.33 mmol) in THF (3 mL) was added to a suspension of NaH (27 mg, 0.66 mmol) in THF at 0° C. and stirred for 30 min at the same temperature. Methyl iodide (58 mg, 0.41 mmol) was added to the above mixture. The reaction mixture was stirred at rt for 2 h. The reaction mixture was poured into ice water and extracted with EtOAc (2×50 mL). The combined organic phases were dried over NaSO4, filtered and concentrated to give (E)-methyl 1-methyl-2-oxo-1′-(3-(2-(trifluoromethyl)phenyl)acryloyl)spiro[indoline-3,4′-piperidine]-5-carboxylate (90 mg, 58%). 1H NMR (CD3OD): 1.85-2.02 (m, 4H), 3.26 (s, 3H), 3.88 (s, 3H), 3.95 (m, 1H), 4.15 (m, 1H), 4.28 (m, 1H), 7.10 (m, 1H), 7.26 (m, 1H), 7.52 (m, 1H), 7.68 (m, 1H), 7.77 (m, 1H), 8.06 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383629B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-84b61d96a56543f4b89782f225e0e673
출처 메모uspto-grants-2013_02