HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Benzyl 3-(hydroxymethyl)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 57275154 | HCID 57275154 | — |
| Product | Benzyl 3-(hydroxymethyl)piperidine-1-carboxylate | HCID 2776577 | 87% |
Reaction Steps
To a solution of 2-naphthalene sulfonyl-serine (prepared in Example XII Part D) (0.78 g, 2.67 mmol) and HOBT (0.4 g, 2.93 mmol) in 11 mL DMF was added WSC (0.56 g, 2.93 mmol), followed by Part D compound (1.03 g, 2.67 mmol). After 5 minutes, NMM (0.82 mL, 5.86 mmol) was added to adjust the pH to 7.5-8.0 and the reaction stirred at room temperature for 16 hrs. The reaction mixture was partitioned between EtOAc and a sat. solution of NaHCO3 and the EtOAc layer was washed with a sat. solution of KHSO4, brine, dried over Na2SO4. The organic layer was concentrated in vacuo to give title compound (87% yield). ##STR126##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05741792 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-3e4977212ad24aaabecdf8bdc3f87594 |
| Source note | uspto-grants-1998_04 |