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HRID 26511作成日:2026年10月25日

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

https://huagongshe.com/reaction/26511

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Benzyltrimethylammonium hydroxideHCID 66854—
反応物3-methylthio-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323406—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物11-methylene-3-methylthio-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323409—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04150139
出典データセットuspto-grants-1979_04
ORD IDord-22b338e3d06e4891a3d85666cc0ffccb
出典メモuspto-grants-1979_04