Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzene, 1-isocyanato-2-methoxy- | HCID 69695 | — |
| Reactant | HCID 86752714 | HCID 86752714 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86752716 | HCID 86752716 | — |
Reaction Steps
Benzyl (R)-4-amino-4-(4-(2-chlorophenyl)-2-ethyl-6H-thieno[3,2-f] [1,2,4]triazolo[4,3-a] [1,4]diazepin-9-yl)butanoate di-p-toluenesulfonate (2.0 g) and 2-methoxyphenyl isocyanate (0.34 ml) were dissolved in DMF (20 ml). Triethylamine (0.97 ml) was added and the mixture was stirred. Water was added to the reaction mixture. The mixture was washed with an aqueous citric acid solution, saturated brine, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel column chromatography using ethyl acetate as an eluent to give 1.19 g of benzyl (R)-4-(4-(2-chlorophenyl)-2-ethyl-6H-thieno[3,2-f] [1,2,4]triazolo[4,3-a] [1,4]diazepin-9-yl)-4-(3-(2-methoxyphenyl)ureido)butanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05760032 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-f0e8b9b35ab5422aa5f339ef9af95ece |
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| Source note | uspto-grants-1998_06 |
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