Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | GYKI-53655 | HCID 126758 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54300912 | HCID 54300912 | 79.7% |
Reaction Steps
After adding 0.5 ml (8.5 mmol) of methyl isocyanate to 0.6 g (1.7 mmol) of 1-(4-aminophenyl)-3-methylcarbamoyl-4-methyl-7,8-methylenedioxy-3,4-dihydro-5H-2,3-benzodiazepine (see Example 98) dissolved in 45 ml of anhydrous dichloromethane, the reaction mixture was stirred at 25 ° C. for 6 days. Then the crystalline precipitate was filtered, washed with 3×2 ml of dichloromethane and.dried at 60° to 80° C. to obtain 0.55 g (79.7%) of the pure aimed product, m.p.: 181°-183° C.,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05604223 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-a4ae4bf1fa154ae6b8313faffbc562cd |
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| Source note | uspto-grants-1997_02 |
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