Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746848Generated: October 31, 2026

Potassium Iodide → {[(cyclohexyloxy)carbonyl]oxy}methyl (2R)-3-[1-amino-7-(trifluoromethoxy)isoquinolin-6-yl]-2-[(3S)-2-oxo-3-({[2-(pyrrolidin-1-yl)-1,3-thiazol-5-yl]sulfonyl}amino)pyrrolidin-1-yl]propanoate

https://huagongshe.com/reaction/1746848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantChloromethyl cyclohexyl carbonateHCID 13603586—
Reactant(R)-3-(1-Amino-7-trifluoromethoxy-isoquinolin-6-yl)-2-[(S)-2-oxo-3-(2-pyrrolidin-1-yl-thiazole-5-sulfonylamino)-pyrrolidin-1-yl]-propionic acid hydrochlorideHCID 71584487—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product{[(cyclohexyloxy)carbonyl]oxy}methyl (2R)-3-[1-amino-7-(trifluoromethoxy)isoquinolin-6-yl]-2-[(3S)-2-oxo-3-({[2-(pyrrolidin-1-yl)-1,3-thiazol-5-yl]sulfonyl}amino)pyrrolidin-1-yl]propanoateHCID 89644321—

Reaction Steps

To a solution of (2R)-3-[1-amino-7-(trifluoromethoxy)isoquinolin-6-yl]-2-[(3S)-2-oxo-3-({[2-(pyrrolidin-1-yl)-1,3-thiazol-5-yl]sulfonyl}amino)pyrrolidin-1-yl]propanoic acid hydrochloride (compound of example 4) (0.5 g, 0.73 mmol) in anhydrous DMF (3 ml) were added potassium carbonate (0.3 g, 2.2 mmol) and chloromethyl cyclohexyl carbonate (0.21 g, 1.1 mmol), followed by potassium iodide (12 mg, 0.07 mmol). The reaction mixture was stirred at room temperature under nitrogen for 12 hours, and then was poured onto cold water, the resulting precipitate was filtered of, washed with water and dried under P2O5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150544B2
Source datasetuspto-grants-2015_10
ORD IDord-dbf50bf2425e4fb193a2b250ee81a6fe
Source noteuspto-grants-2015_10