HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → HCID 12404529, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 57147673 | HCID 57147673 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12404529 | HCID 12404529 | — |
Reaction Steps
Pure gaseous dimethylamine free, in particular, from methylamine, is fed for 2 hours at room temperature, with stirring, into a suspension of 3.85 (0.01 mole) of 6-(o-fluorophenyl)-8-chloro-4H-s-triazolo[1,5-a][1,4]benzodiazepine-2-carboxylic acid ethyl ester [cp. Example 2 (a)-(c)] in 200 ml of methanol. The clear reaction mixture is concentrated in vacuo to dryness. After recrystallisation from isopropanol, the residue yields pure N,N-dimethyl-6-(o-fluorophenyl)-8-chloro-4H-s-triazolo[1,5-a][1,4]benzodiazepine-2-carboxamide, M.P. 180°-182°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04111950 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-161b4e2a041140409fca607ddcbc4a2e |
| Source note | uspto-grants-1978_09 |