Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | HCID 69414377 | HCID 69414377 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69414529 | HCID 69414529 | — |
Reaction Steps
To a cooled (0° C.), stirred solution of 4-BOC-aminomethyl-piperidin-4-ol (0.35 g, 1.52 mmol) in dried CH2Cl2 (5 mL), under N2 was slowly added CBZ-Cl (0.24 mL, 1.67 mmol), followed by triethylamine (0.42 mL, 3.04 mmol). The ice bath was removed and the reaction solution was stirred to rt in 1 h, then concentrated in vacuo. The residue was purified by silica gel chromatography (10 CH2Cl2: 1–20 IPA: 89–10 hexane)) to give 4-BOC-aminomethyl-1-CBZ-piperidin-4-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07217716B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-9cd6b8639c454e44a71b5a56dd8571af |
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| Source note | uspto-grants-2007_05 |
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