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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890930Generated: October 29, 2026

Tetrahydrofuran → HCID 69623716, compound

https://huagongshe.com/reaction/890930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium cyanateHCID 11378442—
ReactantHCID 69623693HCID 69623693—
SolventWaterHCID 962—
ProductHCID 69623716HCID 6962371687%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of N-(propylsulfonyl)-D-isoleucyl-3-(methylamino)-N1-(4-cyanobenzyl)-L-alaninamide (500 mg, 1.0 mmol) in water (1.3 ml)/tetrahydrofuran (3 ml), potassium cyanate (243 mg, 3 mmol) was added under stirring at 50° C. and then further stirred under the same conditions. After stirring for 3 hours, water was added to the reaction mixture, which was then extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous magnesium sulfate. Magnesium sulfate was filtered off and the filtrate was concentrated under reduced pressure to give N-(propylsulfonyl)-D-isoleucyl-3-[(aminocarbonyl)(methyl)amino]-N1-(4-cyanobenzyl)-L-alaninamide (430 mg, 0.87 mmol; yield 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001887B2
Source datasetuspto-grants-2006_02
ORD IDord-4ad74b1acf7040bd96cb9f6e56f0d6db
Source noteuspto-grants-2006_02