Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2,3,3,3-Pentafluoropropylamine | HCID 79002 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | HCID 21091545 | HCID 21091545 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 58655531 | HCID 58655531 | — |
Reaction Steps
In an inert atmosphere and under exclusion of moisture, a solution of 95 mg (0.34 mmol) of (S)—N-((6R,7S)-6,9-dimethyl-8-oxo-6,7,8,9-tetrahydro-5-oxa-9-aza-benzocyclohepten-7-yl)-2-hydroxy-propionamide in 1 ml of toluene was treated with 0.57 ml (0.41 mmol) of triethylamine and 70.9 mg (0.34 mmol) of 4-nitrophenyl chloroformate at room temperature. After stirring at room temperature during the weekend, 0.374 ml (0.34 mmol) of 2,2,3,3,3-pentafluoropropylamine were added and stirring was continued overnight. The solvent was removed by distillation and the crude product was chromatographed on silica gel using a gradient of a 1:3- to 3:1-mixture of ethyl acetate and heptane as the eluent. There were obtained 28 mg (18% of theory) of the title compound as a colourless oil, MS m/e (%): 454.4 (M+H+, 100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07211573B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-1a1f84bd278340099578aae68179f065 |
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| Source note | uspto-grants-2007_05 |
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