HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → HCID 13175695, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 13175737 | HCID 13175737 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13175695 | HCID 13175695 | 45.3% |
Reaction Steps
1 g of 7-chloro-1-(β-chloroethyl)-2-chloromethyl-5-(2-furyl)-2,3-dihydro-1H-1,4-benzodiazepine in 40 ml of methanol is left to react with 0.8 g of methylamine at 50° C. for 3 hours. The reaction mixture is then worked up as described in Example 7. On purification by chromatography, the fractions containing the more highly polar title compound are separated off. 0.4 g of 1,2,3,4,4a,5-hexahydro-9-chloro-3-methyl-7-(2-furyl)-pyrazino[1,2-a][1,4]benzodiazepine is obtained therefrom.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04594436 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-332506155c254eeab1ee8e65a2e61c4c |
| Source note | uspto-grants-1986_06 |