HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 4-formylpiperidine-1-carboxylate → HCID 18328903, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 4-formylpiperidine-1-carboxylate | HCID 1514430 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Pyrimidine, 2-methyl-4-(1-piperazinyl)-, hydrochloride (1:2) | HCID 18328942 | — |
| Solvent | Acetic acid methanol | HCID 10129899 | — |
| Product | HCID 18328903 | HCID 18328903 | 24.1% |
Reaction Steps
To a solution of 1-(tert-butoxycarbonyl)-4-(formyl)piperidine (7.14 g) and 1-(2-methylpyrimidin-4-yl)piperazine dihydrochloride (8.38 g) in methanol/acetic acid (99:1) (150 ml) was added sodium cyanoborohydride (6.32 g) portionwise over 30 minutes and the resultant suspension stirred at arnbient temperature for 3 hours. The suspension was quenched by addition of saturated aqueous sodium bicarbonate solution and the resulting mixture extracted with ethyl acetate. The organic phase was dried (Na2SO4) and evaporated. The residue was purified by chromatography eluting with 5% methanol in dichloromethane to give 1-tert-butoxycarbonyl-4-[1-(2-methylpyrimidin-4-yl)piperazin-4-ylmethyl]piperidine (3.02 g) as a foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06335341B1 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-0ab5f0d385e94395a29e5583357d3447 |
| Source note | uspto-grants-2002_01 |