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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289823Generated: November 1, 2026

Triethylamine → HCID 16658527, compound

https://huagongshe.com/reaction/2289823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,4-Dichloroisoquinoline-7-sulfonyl chlorideHCID 16658294—
Reactanttert-Butyl (R)-2-piperidinecarboxylateHCID 21969834—
SolventDichloromethaneHCID 6344—
ProductHCID 16658527HCID 1665852778.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093731
Source datasetuspto-grants-2000_07
ORD IDord-d4f84f249714427d9a75158b0c72eb88
Source noteuspto-grants-2000_07