HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 4-aminomethyl-4-fluoropiperidine-1-carboxylate → tert-Butyl 4-[(3-ethoxycarbonylisoxazol-5-ylmethoxy-carbonylamino)methyl]-4-fluoropiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 4-aminomethyl-4-fluoropiperidine-1-carboxylate | HCID 40152119 | — |
| Reactant | Ethyl 5-(4-nitrophenoxycarbonyloxymethyl)isoxazole-3-carboxylate | HCID 66661006 | — |
| Product | tert-Butyl 4-[(3-ethoxycarbonylisoxazol-5-ylmethoxy-carbonylamino)methyl]-4-fluoropiperidine-1-carboxylate | HCID 66661123 | 25.5% |
Reaction Steps
The process is performed according to the procedure described in Example 1 (step 1.6.). Starting with 0.70 g (3.01 mmol) of tert-butyl 4-aminomethyl-4-fluoropiperidine-1-carboxylate (commercial) and 1.11 g (3.31 mmol) of ethyl 5-(4-nitrophenoxycarbonyloxymethyl)isoxazole-3-carboxylate, obtained in step 14.1., 0.33 g of pure product is obtained in the form of an orange-coloured oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08716289B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-90508ecd6652446db56b1ffcf62fc5e7 |
| Source note | uspto-grants-2014_05 |