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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436049Generated: October 29, 2026

Ammonia → (r/s)-3-(Tert-butoxycarbonyl)amino-1-(1-amino-4-chloro-5-isoquinolinesulfonyl)-pyrrolidine

https://huagongshe.com/reaction/1436049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPotassium CarbonateHCID 11430—
Reactant(r/s)-3-(Tert-butoxycarbonyl)amino-1-(1,4-dichloro-5-isoquinolinesulfonyl)pyrrolidineHCID 87322862—
Solvent1,3-Dimethyl-2-imidazolidinoneHCID 6661—
SolventSodium chloride; waterHCID 57417360—
Product(r/s)-3-(Tert-butoxycarbonyl)amino-1-(1-amino-4-chloro-5-isoquinolinesulfonyl)-pyrrolidineHCID 67243409—

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of Intermediate 26 (0.20 g), and potassium carbonate (0.31 g) in 1,3-dimethyl-2-imidazolidinone (3 ml, Tokyo Kasei Kogyo) is added with 25% aqueous ammonia (2 ml), and the mixture is stirred at 80° C. for 24 hours in a sealed tube. The reaction mixture is added with saturated brine (30 ml), and extracted 3 times with chloroform (30 ml for each time). The combined organic layer is washed twice with saturated brine (50 ml for each time), and dried over anhydrous magnesium sulfate. The solvent is evaporated under reduced pressure, and the residue is purified by silica gel chromatography (chloroform:methanol=9:1) to obtain the title compound (64.4 mg (predictive yield)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618984B2
Source datasetuspto-grants-2009_11
ORD IDord-cdeff63ba2e94216868c9acc8f1098ae
Source noteuspto-grants-2009_11