Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isopropyl isocyanate | HCID 61277 | — |
| Reactant | Benzyl 4-Hydroxy-1-piperidinecarboxylate | HCID 2794620 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 118037353 | HCID 118037353 | — |
Reaction Steps
Benzyl 4-hydroxypiperidine-1-carboxylate (65 μL), is dissolved in tetrahydrofurane (2 mL), treated with triethylamine (890 μL) and 2-isocyanatopropane (420 μL) and the mixture is stirred for 12 hours at 80° C. Then the mixture is partitioned between saturated aqueous NH4Cl solution and ethylacetate and the organic phase is washed with brine and dried (MgSO4). The solvents are evaporated in vacuo and the residue is purified by HPLC on reversed phase to give the title compound. LC (method 1): tR=1.01 min; Mass spectrum (ESI+): m/z=321 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187477B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-34d25a9416644310abfa62331a2bfc7a |
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| Source note | uspto-grants-2015_11 |
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