HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26511Generated: October 23, 2026
Formaldehyde → 11-methylene-3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine
https://huagongshe.com/en/reaction/26511
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | 3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine | HCID 21323406 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 11-methylene-3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine | HCID 21323409 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04150139 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-22b338e3d06e4891a3d85666cc0ffccb |
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| Source note | uspto-grants-1979_04 |
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