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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26511생성일: 2026년 10월 24일

Formaldehyde → 11-methylene-3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine

https://huagongshe.com/ko/reaction/26511

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Benzyltrimethylammonium hydroxideHCID 66854—
반응물3-methylthio-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323406—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물11-methylene-3-methylthio-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323409—

반응 단계

To 4.6 g of 3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine in 60 ml of tetrahydrofuran was added 2.4 g of paraformaldehyde together with 4.0 ml of a 40% solution of trimethylbenzylammonium hydroxide in methanol. After refluxing the mixture for 30 minutes, the solvent was evaporated off. The residue was diluted with water and extracted with ethyl acetate. The ethyl acetate layer was washed with water and dried over Na2SO4. The solvent was then evaporated off and the residual crystals were collected by filtration, washed with isopropyl alcohol and dried. The above procedure provided 11-methylene-3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine as crystals. Recrystallization from ethyl acetate yielded colorless needles melting at 121°-122° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04150139
출처 데이터셋uspto-grants-1979_04
ORD IDord-22b338e3d06e4891a3d85666cc0ffccb
출처 메모uspto-grants-1979_04