Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 12318099 | HCID 12318099 | — |
| Product | HCID 23317224 | HCID 23317224 | — |
Reaction Steps
500 mg of 3,8-dichloro-1-methyl-6-phenyl-1,2,3,4-tetrahydro-1,5-benzodiazocine hydrochloride were heated in a solution of 110 mg sodium in 70 ml methanol under reflux for 12 hours. After evaporation of the methanol in a vacuum the mass was further processed with water/chloroform and the chloroform solution was evaporated and concentrated in a vacuum. The residue was taken up in isopropanol and reacted with an ether solution of hydrogen chloride. There was obtained 7-chloro-1-methyl-2-methoxymethyl-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepine hydrochloride which product also was identical with the product obtained directly by reaction of N-methyl-N-(2-hydroxy-3-benzoylaminopropyl)-4'-chloroaniline in phosphoroxychloride at 120° C. and subsequent reaction with sodium and methanol as disclosed in Examples 4 and 8 of application Ser. No. 355 986; m.p. 198°-210° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04595531 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-9d1a9a0bfd9042909f99bce13c6023a3 |
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| Source note | uspto-grants-1986_06 |
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