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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737737Generated: November 1, 2026

Phenyl isocyanate → HCID 22611604, compound

https://huagongshe.com/reaction/1737737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
ReactantTriethylamineHCID 8471—
ReactantHCID 86751892HCID 86751892—
SolventDichloromethaneHCID 6344—
ProductHCID 22611604HCID 2261160470%

Reaction Steps

To a solution of 2.0 gm (5.74 mMol) 5-amino-3-(1-methylpiperidin-4-yl)-1H-indole dihydrochloride mono-ethanolate and 5.0 mL (36 mMol) triethylamine in 100 mL dichloromethane were added 1.37 mL (12.6 mMol) phenyl isocyanate. The reaction mixture was stirred for 15 minutes and was then washed with 100 mL of water. The remaining organics were dried over sodium sulfate and concentrated under reduced pressure. The resultant residue was crystallized from acetonitrile to give 1.40 gm (70%) N-phenyl-N'-(3-(1-methylpiperidin-4-yl)-1H-indol-5-yl)urea. This material was dissolved in methanol and to it was added an equivalent of methanolic hydrogen chloride. The solution was then concentrated under reduced pressure and the residual oil crystallized from ethanol to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962474
Source datasetuspto-grants-1999_10
ORD IDord-fee1595b4eb8450a9121c970942c5fd4
Source noteuspto-grants-1999_10