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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289809Generated: October 29, 2026

Triethylamine → N-[(1,4-dichloro-7-isoquinolinyl)sulphonyl]-D-valine t-butyl ester

https://huagongshe.com/reaction/2289809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-butyl D-valinateHCID 6931638—
Reactant1,4-Dichloroisoquinoline-7-sulfonyl chlorideHCID 16658294—
SolventDichloromethaneHCID 6344—
ProductN-[(1,4-dichloro-7-isoquinolinyl)sulphonyl]-D-valine t-butyl esterHCID 1665880772.2%

Reaction Conditions

Temperature23 °C

Reaction Steps

D-Valine t-butyl ester (354 mg, 1.69 mmol) and then NEt3 (0.59 mL, 4.2 mmol) were added to a stirred solution of 1,4-dichloro-7-isoquinolinesulphonyl chloride (500 mg, 1.69 mmol) and in CH2Cl2 (20 mL) and the mixture was stirred at 23° C. for 16 h. The mixture was diluted with CH2Cl2 (50 mL), washed with saturated aqueous NaHCO3, water, aqueous citric acid (1 M), water, brine, dried (MgSO4) and evaporated in vacuo. The residue was dissolved in i-Pr2O and hexane was added which gave a precipitate. The solvents were evaporated in vacuo and the solid was triturated with hexane to give N-[(1,4-dichloro-7-isoquinolinyl)sulphonyl]-D-valine t-butyl ester (532 mg, 1.22 mmol) as a white solid. An analytical sample was obtained by recrystallisation from hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093731
Source datasetuspto-grants-2000_07
ORD IDord-cda5791dde4d4c8fb06bd8b789694eee
Source noteuspto-grants-2000_07