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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379755Generated: November 1, 2026

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

https://huagongshe.com/reaction/2379755

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—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
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 (0.2 6 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 numberUS05364856
Source datasetuspto-grants-1994_11
ORD IDord-f905be862cde46c29e2ba534343e73d2
Source noteuspto-grants-1994_11