HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 86687859, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(Chloromethyl)benzoyl chloride | HCID 70136 | — |
| Reactant | 5-Hexyn-1-ol | HCID 70234 | — |
| Reactant | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86687859 | HCID 86687859 | — |
Reaction Steps
To a solution of 4-(chloromethyl)benzoyl chloride (2.00 g; 10.6 mmol) in THF (30 ml) are added 5-hexyn-1-ol (1.18 ml; 10.6 mmol) and DMAP (0.1 g; 0.82 mmol). The mixture is refluxed overnight with stirring. BOC-4-aminopiperidine (2.33 g; 11.6 mmol) and triethylamine (3.24 ml; 23.3 mmol) are added and the mixture is refluxed for further 3 h. Ethyl acetate (200 ml) and water (50 ml) are added. The organic layer is separated, washed with water and with brine and evaporated to dryness. The residue is purified by silica gel column chromatography (gradient cyclohexane/ethyl acetate 8:2→2:8) to yield 5-Hexyn-1-yl 4-[(4-{[(tertbutoxy)carbonyl]amino}piperidin-1-yl)methyl]-benzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859559B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-5aa7b02a1c884fe8844357a2db821a01 |
| Source note | uspto-grants-2014_10 |