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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426241Generated: October 26, 2026

2-Bromopropanedial → 6-Bromo-2-tert-butyl-[1,2,4]triazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/1426241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopropanedialHCID 74945—
ReactantHCID 178441978HCID 178441978—
SolventAcetic AcidHCID 176—
Product6-Bromo-2-tert-butyl-[1,2,4]triazolo[1,5-a]pyrimidineHCID 5831670483%

Reaction Conditions

Temperature60 °C

Reaction Steps

3-tert-Butyl-1H-1,2,4-triazol-5-amine (CAS 202403-45-0) (35%, 13 g, 32.5 mmol) was dissolved in acetic acid (50 ml) and 2-bromomalonaldehyde (7.35 g, 48.7 mmol, 1.5 equiv.) was added. The reaction mixture was stirred for 3 hours at 60° C. The reaction mixture was evaporated and neutralized with saturated NaHCO3 solution 2N and extracted two times with dichloromethane. The organic extracts were dried with sodium sulfate, filtered and evaporated to dryness. The crude product was purified by flash chromatography on 70 g silica gel (heptane:EtOAc 100:0→50:50). The desired 6-bromo-2-tert-butyl-[1,2,4]triazolo[1,5-a]pyrimidine (6.83 g, 83% yield) was obtained as a white solid, MS: m/e=255.0/257.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933094B2
Source datasetuspto-grants-2015_01
ORD IDord-e974ab5de4244303af9248ca0ef34c61
Source noteuspto-grants-2015_01