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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179090Generated: October 31, 2026

3-(Bromomethyl)-4-methyl-1,2,5-oxadiazole → HCID 89586244, compound

https://huagongshe.com/reaction/2179090

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Bromomethyl)-4-methyl-1,2,5-oxadiazoleHCID 19832741—
Reactant5-tert-Butyl-7-(3,3-difluoro-pyrrolidin-1-yl)-2-ethyl-2H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 71576307—
ReactantHCID 178441794HCID 178441794—
ProductHCID 89586244HCID 89586244—

Reaction Steps

In analogy to the procedure described for the synthesis of 5-tert-butyl-7-(3,3-difluoro-pyrrolidin-1-yl)-2-ethyl-2H-[1,2,3]triazolo[4,5-d]pyrimidine (example 3, step b), the title compound was prepared from 5-tert-Butyl-7-(3,3,4,4-tetrafluoro-pyrrolidin-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine and 3-(bromomethyl)-4-methyl-1,2,5-oxadiazole and isolated as light yellow gum. MS (m/e): 415.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067943B2
Source datasetuspto-grants-2015_06
ORD IDord-855df7300fee47dfb1703eee9ff5dc6d
Source noteuspto-grants-2015_06