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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289812Generated: October 26, 2026

Triethylamine → Methyl 1-{[(1,4-dichloro-7-isoquinolinyl)sulphonyl]amino}-cyclohexanecarboxylate

https://huagongshe.com/reaction/2289812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 1-aminocyclohexanoateHCID 4048819—
Reactant1,4-Dichloroisoquinoline-7-sulfonyl chlorideHCID 16658294—
SolventDichloromethaneHCID 6344—
ProductMethyl 1-{[(1,4-dichloro-7-isoquinolinyl)sulphonyl]amino}-cyclohexanecarboxylateHCID 1665802722.9%

Reaction Conditions

Temperature23 °C

Reaction Steps

A mixture of methyl 1-aminocyclohexanecarboxylate (325 mg, 1.68 mmol), NEt3 (0.49 mL, 3.5 mmol) and 1,4-dichloro-7-isoquinolinesulphonyl chloride (415 mg, 1.40 mmol) in CH2Cl2 (30 mL) was stirred at 23° C. for 16 h. The mixture was diluted with CH2Cl2, washed with dilute HCl (2 M), saturated aqueous NaHCO3, brine, dried (Na2SO4) and evaporated in vacuo. The residue was purified by column chromatography upon silica gel using hexane-EtOAc (80:20 to 70:30) as eluant, followed by trituration with i-Pr2O, to give to give methyl 1-{[(1,4-dichloro-7-isoquinolinyl)sulphonyl]amino}-cyclohexanecarboxylate (132 mg, 0.32 mmol) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093731
Source datasetuspto-grants-2000_07
ORD IDord-e996a60fd7694cab959b77ab7542a524
Source noteuspto-grants-2000_07