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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042190Generated: October 26, 2026

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

https://huagongshe.com/reaction/2042190

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 numberUS08586581B2
Source datasetuspto-grants-2013_11
ORD IDord-fa526b174780448899ab0de91aaf5e3f
Source noteuspto-grants-2013_11