HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 12050645, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Boc-4-Cbz-amino-piperidine | HCID 1514305 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12050645 | HCID 12050645 | 109.9% |
Reaction Steps
Sodium hydride (47 mg of 60% oil dispersion, 1.2 mmol) was added to a solution of 4-(benzyloxycarbonylamino)-1-(tert-butoxycarbonyl)piperidine (200 mg, 0.598 mmol) from Procedure 4, Step C and allyl bromide (0.251 mL, 351 mg, 2.9 mmol) in 2.0 mL of DMF, and the reaction was stirred overnight at rt. The reaction mixture was poured into 20 mL of water and extracted with 3×20 mL of ethyl ether. The combined organic layers were washed with 30 mL of brine, dried over sodium sulfate, and evaporated. The crude product was purified by FC on silica gel, eluting with 20% ethyl acetate in hexane, to give 246 mg of the title compound as a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06506777B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-7a1daf98f4144e0daf75b44076fbd2f0 |
| Source note | uspto-grants-2003_01 |