Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | HCID 67440367 | HCID 67440367 | — |
| Reactant | HCID 178518668 | HCID 178518668 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11527103 | HCID 11527103 | 58.8% |
Reaction Steps
Triethylamine (43 μL, 0.310 mmol) was added to a solution of the bis hydrochloride salt of (6S,9R)-6-(2,3-difluorophenyl)-3-(tetrahydrofuran-3-yl)-6,7,8,9-tetrahydro-5H-imidazo[1,2-a]azepin-9-amine (42 mg, 0.103 mmol) and 4-nitrophenyl chloroformate (21 mg, 104 mmol) in tetrahydrofuran (3 mL) at 0° C. After 30 min, 2-oxo-1-piperidinium-4-yl-2,3-dihydro-1H-imidazo[4,5-b]pyridin-4-ium dichloride (45 mg, 0.155 mmol), triethylamine (43 μL, 0.310 mmol) and dichloromethane (3 mL) were added and the mixture allowed to warm to ambient temperature. After 18 h, the reaction was concentrated. Purification by reverse phase HPLC (C-18, 90% water/acetonitrile→100% acetonitrile with 0.1% trifluoroacetic acid) gave the title compound (35 mg). MS 578.2702 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039460B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-36cf92b3bd244bf1ad500405caa02920 |
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| Source note | uspto-grants-2011_10 |
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