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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719785Generated: October 29, 2026

Ethyl isocyanate → HCID 21887008, compound

https://huagongshe.com/reaction/719785

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 numberUS07132547B2
Source datasetuspto-grants-2006_11
ORD IDord-0f8659fe04a141bd976a53096fd992c2
Source noteuspto-grants-2006_11