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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154014Generated: October 27, 2026

1-Pyrrolidineethanamine → 6-[2-(1-Pyrrolidinyl)ethylamino]-7,8,9,10-tetrahydro-1,2,4-triazolo[3,4-a]phthalazine

https://huagongshe.com/reaction/1154014

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PyrrolidineethanamineHCID 1344—
Reactant6-Chloro-7,8,9,10-tetrahydro-[1,2,4]triazolo[3,4-a]phthalazineHCID 12622441—
Solvent2-MethoxyethanolHCID 8019—
Product6-[2-(1-Pyrrolidinyl)ethylamino]-7,8,9,10-tetrahydro-1,2,4-triazolo[3,4-a]phthalazineHCID 13365588—

Reaction Steps

A solution of 5.0 g of 6-chloro-7,8,9,10-tetrahydro-1,2,4-triazolo[3,4-a]phthalazine and 10.0 g of 1-(2-aminoethyl)pyrrolidine in 50 ml of 2-methoxyethanol was heated at reflux for 15 hours. The solution was then concentrated and the resulting residue was partitioned between methylene chloride and saturated aqueous sodium bicarbonate solution. The organic layer was separated, dried over sodium sulfate and concentrated. The concentrate was triturated with ether and the solid which formed was separated by filtration to give 6-[2-(1-pyrrolidinyl)ethylamino]-7,8,9,10-tetrahydro-1,2,4-triazolo[3,4-a]phthalazine melting at about 160°-162° C. after recrystallization from a mixture of toluene and hexane. This compound has the following structural formula ##STR3##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04487930
Source datasetuspto-grants-1984_12
ORD IDord-dde6ebfad6b342e69b42e8d97b5b3168
Source noteuspto-grants-1984_12