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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924841Generated: October 31, 2026

Triethylamine → [(2-Chloroethyl)amino]-n-(4-fluoroindanyl)carboxamide

https://huagongshe.com/reaction/1924841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloroethyl isocyanateHCID 16035—
Reactant4-fluoro-2,3-dihydro-1H-inden-1-amineHCID 16244318—
SolventDichloromethaneHCID 6344—
Product[(2-Chloroethyl)amino]-n-(4-fluoroindanyl)carboxamideHCID 5935577233.9%

Reaction Steps

To a stirred, cold (0° C.) solution of 7.0 grams (0.046 mole) of 4-fluoroindanylamine (known compound) and 5.7 grams (0.056 mole) of triethylamine in 100 mL of methylene chloride was added 5.4 grams (0.051 mole) of 2-chloroethyl isocyanate. The cold reaction mixture was stirred for three hours at which time it was filtered. The filter cake was rinsed with methylene chloride. The filtrates were combined and concentrated under reduced pressure to a residue. The residue was triturated with hexanes and the mixture filtered. The filter cake was dried under reduced pressure to yield 4.0 grams of [(2-chloroethyl)amino]-N-(4-fluoroindanyl)carboxamide. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178567B2
Source datasetuspto-grants-2012_05
ORD IDord-1646a22f78fb499d8946714d0c3cae23
Source noteuspto-grants-2012_05