HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 23317233, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 12318108 | HCID 12318108 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 23317233 | HCID 23317233 | — |
Reaction Steps
A solution of 1 g of 8-chloro-1-methyl-3-hydroxy-6-phenyl-1,2,3,4-tetrahydro-1,5-benzodiazocine in 50 ml benzene was heated under reflux for 1 hour with 1 ml thionylchloride. The solution was reacted with a few drops of triethylamine, washed with water and concentrated by evaporation to dryness in a vacuum. The residue was dissolved in isopropanol and reacted with an ether solution of hydrogen chloride. There was obtained 7-chloro-1-methyl-2-chloromethyl-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepine hydrochloride. The product was also identical with the product obtained in Example 10 of application Ser. No. 335,986; m.p. 110°-112° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04595531 |
| Source dataset | uspto-grants-1986_06 |
| ORD ID | ord-86de0b4f6d224fd88f0edacaf1fbc5b5 |
| Source note | uspto-grants-1986_06 |