HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → 3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraen-1-yl 4-methylpiperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Geranylgeraniol | HCID 5281365 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraen-1-yl 4-methylpiperazine-1-carboxylate | HCID 78164056 | 88% |
Reaction Steps
To a solution of alcohol 1 (160 mg, 55 mmol) in DCM (3 mL) at 0° C. was added carbonyldiimidazole (CDI) (107 mg, 0.66 mmol) and the reaction was stirred for 1 h. Then N-methylpiperazine (80 mg, 0.72 mmol) and DMAP (68 mg, 0.55 mmol) were added and stirred for 12 h. Solvent was removed and the residue was purified by column chromatography (DCM/MeOH) to give the carbamate 40a as a viscous oil in 88% yield (191 mg). TLC Rf: 0.54 (10% MeOH/DCM); 1H NMR (300 MHz, CDCl3): δ 5.34 (t, 3H), 5.08 (m, 3H), 4.59 (d, 2H), 3.49 (m, 4H), 2.35 (m, 4H), 2.29 (s, 3H), 2.10-1.97 (m, 12H), 1.70 (s, 3H), 1.67 (s, 3H), 1.59 (s, 9H); LCMS: MS (m/z): 417 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045403B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-1050e955b60e4cccaf3b383301c65a72 |
| Source note | uspto-grants-2015_06 |