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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 627895생성일: 2026년 10월 26일

Water → N-(2-chlorophenyl)-N-methyl-4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepin-2-carboxamide

https://huagongshe.com/reaction/627895

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물N-(2-chlorophenyl)-4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepin-2-carboxamideHCID 57900340—
용매TetrahydrofuranHCID 8028—
생성물N-(2-chlorophenyl)-N-methyl-4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepin-2-carboxamideHCID 4424249567.4%

반응 단계

Sodium hydride, 60% dispersion in mineral oil (80 mg, 2.0 mmol) was added to a solution of N-(2-chlorophenyl)-4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepin-2-carboxamide (71.4 mg, 0.2 mmol) in 10 ml of tetrahydrofuran. The mixture was stirred for 30 min and mixed with methyl iodide (0.12 mL, 2.0 mmol). The reaction mixture was stirred for 1 hour. The mixture was mixed with 50 ml of iced water and extracted with ethyl acetate twice. The combined ethyl acetate solution was washed with brine, dried over MgSO4, concentrated in vacuo, and purified on silica gel column eluting with 25% of ethylacetate in methylene chloride to give 162 (yield 50 mg, 67%). 1H NMR (400 MHz, DMSO) δ 8.57 (s, 1H), 8.25 (d, J=5.5, 1H), 7.68 (t, J=5.9, 2H), 7.60-7.50 (m, 2H), 6.98 (d, J=5.5, 1H), 6.64 (s, 1H), 4.27 (m, 2H), 3.28 (s, 3H), 2.99 (m, 2H). MS (ESI+) 371.1

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09309265B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-7939cf6ee1d84651bd371037677c9460
출처 메모uspto-grants-2016_04