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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 852658생성일: 2026년 10월 27일

Triethylamine → Ethyl 7-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-3-ethyl-1H-indole-5-carboxylate

https://huagongshe.com/reaction/852658

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물ethyl 7-{[(4-chlorobutyl)sulfonyl]amino}-3-ethyl-1H-indole-5-carboxylateHCID 69357263—
용매EthanolHCID 702—
생성물Ethyl 7-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-3-ethyl-1H-indole-5-carboxylateHCID 6936122072.5%

반응 조건

온도70 °C

반응 단계

To a solution of ethyl 7-{[(4-chlorobutyl)sulfonyl]amino}-3-ethyl-1H-indole-5-carboxylate (D242) (230 mg, 0.59 mmol, 1 equiv) in EtOH (10 ml) was added NEt3 (249 μl, 1.78 mmol, 3 equiv) and the resulting solution was stirred at 70° C. for 3 h. NEt3 (1 ml, excess) was added and the solution was stirred at the same temperature for 15 h then cooled to room temperature and concentrated in vacuo. The residue was dissolved in AcOEt and the organic phase was washed with a 2N aqueous HCl solution, dried over MgSO4 and concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (AcOEt/iso-hexane: 3/7) gave ethyl 7-(1,1-dioxidotetrahydro-2H-1,2-thiazin-2-yl)-3-ethyl-1H-indole-5-carboxylate (B148) (150 mg, 72%) as a colorless oil. [M−H]−=349.3, RT=3.10 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07253198B2
출처 데이터셋uspto-grants-2007_08
ORD IDord-b7c60fc36d704f8c98e446e2710f7aa7
출처 메모uspto-grants-2007_08