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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086837Generated: November 1, 2026

Boron tribromide → HCID 178456607, compound

https://huagongshe.com/reaction/1086837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 178456479HCID 178456479—
SolventMethanolHCID 887—
ProductHCID 178456607HCID 17845660744.4%

Reaction Steps

Boron tribromide (0.35 ml) was added to a stirred suspension of 1-benzyl-3-propyl-1,2,3,4-tetrahydro-5H-imidazo [2',1':5,1]pyrazolo[3,4-d]pyrimidine-2,4-dione (0.5 g) at room temperature. The reaction mixture was refluxed for 22 hours and then cooled to room temperature, followed by addition of methanol (10 ml). The mixture was stirred for a while and was concentrated to dryness. After addition of ethyl acetate, resulting crystals were collected by filtration and washed with water to give crude crystals. Recrystallization from ethyl acetate gave colorless crystals (0.16 g, 44%), m.p. 326°-328° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05032594
Source datasetuspto-grants-1991_07
ORD IDord-68a266188b7447ff8ee0f8a9fd055778
Source noteuspto-grants-1991_07