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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052281Generated: October 28, 2026

Hydrochloric Acid → HCID 136005323, compound

https://huagongshe.com/reaction/2052281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant[1,2,4]Triazolo[4,3-a]quinazoline, 7-chloro-1-methyl-5-phenyl-HCID 1869146—
ReactantSodium borohydrideHCID 4311764—
SolventDimethylformamideHCID 6228—
ProductHCID 136005323HCID 13600532357.3%

Reaction Steps

To a suspension of 1.3 g of 7-chloro-1-methyl-5-phenyl-s-triazolo[4,3-a]quinazoline in 70 ml of dimethylformamide was added 0.5 g of sodium borohydride. The mixture was heated with stirring at 75°-80° C. for 2 hours and then poured into ice-water. The resulting mixture was neutralized with dilute hydrochloric acid, and the precipitate formed was collected by filtration and washed with water. The solid was then suspended in a mixture of 40 ml of methanol and 5 ml of concentrated hydrochloric acid, and the mixture was stirred at room temperature for 2 hours. After neutralization with ammonia water, the mixture was extracted with chloroform. The chloroform layer was dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The residue was recrystallized from dimethylformamideethanol to give 0.75 g of 7-chloro-4,5-dihydro-1-methyl-5-phenyl-s-triazolo[4,3-a]quinazoline as colorless needles, m.p. 262°-265° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04183932
Source datasetuspto-grants-1980_01
ORD IDord-7d1b58d5e5dd49e9b91ac0b77b7c893f
Source noteuspto-grants-1980_01