Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Phenyl-5-(trifluoromethyl)-oxazole-4-carboxylic acid | HCID 2776438 | — |
| Reactant | Tert-butyl 4-(4-aminophenyl)-1,4-diazepane-1-carboxylate | HCID 18008968 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59185678 | HCID 59185678 | 83% |
Reaction Steps
A mixture of 2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid (1.0 g, 3.90 mmol), methylene chloride (50 mL), and a catalytic amount of DMF was stirred under argon, and oxalyl chloride (2M in methylene chloride, 2 mL, 4.0 mmol) was dripped into the mixture over 5 min. The mixture was stirred at room temperature for 1.0 hr and the reaction was concentrated to dryness. Benzene was added and the solution was evaporated to dryness again. The white-yellow solid was re-dissolved in methylene chloride (30 mL) and dripped, under argon, into a solution of 4-(4-amino-phenyl)-[1,4]diazepane-1-carboxylic acid tert-butyl ester (1.2 g, 4.0 mmol), and triethylamine (0.6 g, 5.8 mmol) in methylene chloride (50 mL). The reaction was stirred at room temperature for 0.5 hr then concentrated and the residue was taken up in EtOAc (100 mL) and washed with saturated ammonium chloride (100 mL), brine (100 mL) and dried with anhydrous sodium sulfate. The solvent was removed and the residue was purified on a flash column chromatography with EtOAc/hexanes to afford 4-{4-[(2-phenyl-5-trifluoromethyl-oxazole-4-carbonyl)-amino]-phenyl}-[1,4]diazepane-1-carboxylic acid tert-butyl ester (1.65 g, 83% yield) as a white solid. ES-MS for C27H29F3N4O4 calcd. (m/e) 530, observed 531 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08211884B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-1803693df2594b9fa8ad7989aa97405e |
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| Source note | uspto-grants-2012_07 |
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