Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | HCID 70975608 | HCID 70975608 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70975393 | HCID 70975393 | 72.3% |
Reaction Steps
In a dry reaction bottle, 8.32 g triphosgene (28 mmol) and 7.8 mL triethylamine (56 mmol) were added and dissolved in 240 mL tetrahydrofuran. A solution of 5.31 g (R)-1-[2-methoxycarbonyl-5-amino-6-methylaminopyridin-4-yl]piperidine-3-carbamic acid tert-butyl ester (14 mmol) in tetrahydrofuran (80 mL) was added dropwise at −10° C. After addition, the reaction solution was adjusted to be neutral with saturated sodium carbonate solution. Water and dichloromethane were added to the reaction solution. The reaction solution was extracted with dichloromethane. The organic phase was combined, washed with saturated brine, dried with anhydrous sodium sulfate, evaporated to remove dichloromethane, washed with ethyl acetate, filtrated, and dried to afford 4.1 g titled product as white solid, with a yield of 72.3%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680089B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-3acdec0e2f1b4822adf2d68e70fa1817 |
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| Source note | uspto-grants-2014_03 |
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