HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 16658527, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Dichloroisoquinoline-7-sulfonyl chloride | HCID 16658294 | — |
| Reactant | tert-Butyl (R)-2-piperidinecarboxylate | HCID 21969834 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 16658527 | HCID 16658527 | 78.3% |
Reaction Steps
1,4-Dichloro-7-isoquinolinylsulphonyl chloride (245 mg, 0.83 mmol) was added to a solution of tert-butyl 2(R)-piperidine carboxylate (153 mg, 0.83 mmol) and triethylamine (170 μl, 1.22 mmol) in CH2Cl2 (15 ml), and the reaction stirred at room temperature for 18 h. The solution was diluted with CH2Cl2, washed with 2M hydrochloric acid, saturated Na2CO3 solution and then brine, dried (MgSO4), and evaporated in vacuo. The residual oil was purified by column chromatography upon silica gel using an elution gradient of pentane-EtOAc (100:0 to 90:10), to give tert-butyl (2R)-1-[(1,4-dichloro-7-isoquinolinyl)sulphonyl]-2-piperidinecarboxylate, (290 mg, 0.65 mmol) as a colourless film.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093731 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-d4f84f249714427d9a75158b0c72eb88 |
| Source note | uspto-grants-2000_07 |