HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979402Generated: October 29, 2026
Triethylamine → 1-[1-(2-toluoylmethyl)-2-oxo-5-(3,3-dimethylbutanoyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-3-yl]-3-(3-ethoxycarbonylphenyl)urea
https://huagongshe.com/reaction/1979402
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 3-aminobenzoate | HCID 11400 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | 1-(2-toluoylmethyl)-2-oxo-3-amino-5-(3,3-dimethylbutanoyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine | HCID 21201765 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[1-(2-toluoylmethyl)-2-oxo-5-(3,3-dimethylbutanoyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepin-3-yl]-3-(3-ethoxycarbonylphenyl)urea | HCID 21201577 | 165.7% |
Reaction Steps
Ethyl 3-aminobenzoate (236 mg) was dissolved in tetrahydrofuran (40 ml), under ice-cooling triphosgene (140 mg) was added and triethylamine (120 μl) was added thereto five times every 3 minutes, a solution of 1-(2-toluoylmethyl)-2-oxo-3-amino-5-(3,3-dimethylbutanoyl)-8-methyl-1,3,4,5-tetrahydro-2H-1,5-benzodiazepine (536 mg) in tetrahydrofuran (10 ml) was subsequently added, the mixture was stirred for 30 minutes at same temperature,and additionally stirred for 2 hours at room temperature. The reaction mixture was poured into water (400 ml),extracted with methylene chloride (50 ml), and the organic layer was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, the residue was purified by silica gel column chromatography(n-hexane:ethyl acetate=2:1), to thereby obtain 479 mg of the titled compound
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06239131B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-e605156c228e4ac69377375d34e8ad7d |
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| Source note | uspto-grants-2001_05 |
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