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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192827Generated: November 2, 2026

Propane, 1-chloro-3-isocyanato- → HCID 59625599, compound

https://huagongshe.com/reaction/2192827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropane, 1-chloro-3-isocyanato-HCID 166752—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 59625415HCID 59625415—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59625599HCID 59625599—

Reaction Steps

tert-Butyl (3R,5S)-3-amino-5-{[(2-tert-butyl-4-{[3-(methylsulfanyl)propyl]amino}pyrimidin-5-yl)carbonyl](2-methylpropyl)amino}piperidine-1-carboxylate (97 mg) was dissolved in 1,2-dichloroethane (2 ml)-THF (2 ml), chloropropyl isocyanate (25 μl) was added, and the mixture was stirred at room temperature for 1 hr. Potassium tert-butoxide (30 mg) was added and the reaction mixture was stirred at room temperature for 8 hr, and further at 60° C. for 12 hr. The reaction mixture was diluted with water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was dissolved in THF (4 ml), sodium hydride (50% contained, 26 mg) was added under ice-cooling, and the mixture was stirred under ice-cooling for 4 hr. The reaction mixture was diluted with water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, eluted with ethyl acetate-methanol (100:0-90:10) and concentrated under reduced pressure to give the object compound (103 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329691B2
Source datasetuspto-grants-2012_12
ORD IDord-f3efcc96332947baa233988c7b7a1e6b
Source noteuspto-grants-2012_12