Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722930Generated: October 30, 2026

Ethyl isocyanate → HCID 21887008, compound

https://huagongshe.com/reaction/722930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isocyanateHCID 8022—
ReactantHCID 21886799HCID 21886799—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21887008HCID 2188700860.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

Ethyl isocyanate (85 mg) was added to a solution of tert-butyl 5-(2,3-dihydro-1H-indol-5-yl)-5-oxopentyl[2-(2-methoxyphenyl)ethyl]carbamate (362 mg) obtained in Reference Example 50 in tetrahydrofuran (2 ml), and the mixture was stirred at 60° C. for 2 hours. The solvent was evaporated under reduced pressure, water was added to the resulting residue, and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was-purified by silica gel chromatography (eluting solvent; hexane:ethyl acetate=1:1) to give the title compound as a pale yellow oil (254 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138533B2
Source datasetuspto-grants-2006_11
ORD IDord-8fc04fe4eeb54147857bd66b39e3a801
Source noteuspto-grants-2006_11