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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164503Generated: November 1, 2026

Cyclohexyl isocyanate → HCID 20511184, compound

https://huagongshe.com/reaction/1164503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl isocyanateHCID 18502—
ReactantHCID 20511193HCID 20511193—
SolventChloroformHCID 6212—
ProductHCID 20511184HCID 20511184—

Reaction Steps

Cyclohexyl isocyanate (0.5 g.) in dry chloroform (5 ml.) was added dropwise to 6,7-dimethoxy-1-[4-[2-(methylamino)ethyl]piperidino]phthalazine (1.0 g.) in dry chloroform (10 ml.) with stirring and ice-water cooling. After further stirring at room temperature (20°) for 1 hour the mixture was concentrated in vacuo, triturated with minimum quantity of ethyl acetate and filtered. The resultant solid was dissolved in methylene chloride (10 ml.), filtered, treated with ethyl acetate (20 ml.) and gently distilled to remove methylene chloride. The residual ethyl acetate solution was left standing in the refrigerator overnight to precipitate crystalline 6,7-dimethoxy-1-[4-[2-(3-cyclohexyl-1-methylureido)ethyl]piperidino]phthalazine (820 mg.), m.p. 204°-206° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04370328
Source datasetuspto-grants-1983_01
ORD IDord-37c80bcd4d0040b1a8b236c62e812ee2
Source noteuspto-grants-1983_01