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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377627Generated: October 25, 2026

Potassium Carbonate → (4R)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole-6carboxylic hydrazide

https://huagongshe.com/reaction/1377627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant(4S)-6-iodo-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indoleHCID 10691283—
ReactantHCID 178516071HCID 178516071—
CatalystHCID 178418397HCID 178418397—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product(4R)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole-6carboxylic hydrazideHCID 70284014—

Reaction Steps

To a solution of 5.0 g (13.1 mmol) of (4S)-6-iodo-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole in 250 ml of acetonitrile was added 3.5 g (37 mmol) of 2-hydroxypyridine, 16.9 g (122 mmol) of powdered potassium carbonate, and 0.30 g (0.26 mmol) of tetrakis(triphenylphosphine)palladium. The resultant mixture was heated at 65° C. under a carbon monoxide atmosphere for 14 hours. The cooled mixture was then treated with 2 ml of hydrazine hydrate and stirred for another 15 hours. After filtering, the mixture was concentrated in vacuo to provide a residue. This residue was taken up in methylene chloride and extracted with aqueous tartaric acid solution. The aqueous layer was basified with 1M sodium hydroxide solution and the product was extracted into methylene chloride. Evaporation of solvent in vacuo left an oily solid which, after thorough washing with a 1:2 mixture of toluene and hexane, afforded 0.60 g of (4R)-4-(di-n-propylamino)-1,3,4,5-tetrahydrobenz[cd]indole-6-carboxylic hydrazide. m.p. 199°-201° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665743
Source datasetuspto-grants-1997_09
ORD IDord-c1c237270326428296e5dee137cae2ea
Source noteuspto-grants-1997_09