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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179031Generated: October 30, 2026

3-(Bromomethyl)-4-methyl-1,2,5-oxadiazole → 5-tert-Butyl-7-(3,3-difluoro-pyrrolidin-1-yl)-2-(4-methyl-furazan-3-ylmethyl)-2H-[1,2,3]triazolo[4,5-d]pyrimidine

https://huagongshe.com/reaction/2179031

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 178441789HCID 178441789—
Product5-tert-Butyl-7-(3,3-difluoro-pyrrolidin-1-yl)-2-(4-methyl-furazan-3-ylmethyl)-2H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 71576595—

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-difluoropyrrolidin-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): 379.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067943B2
Source datasetuspto-grants-2015_06
ORD IDord-5360ad04f9c542a0be9e60e847a50d1f
Source noteuspto-grants-2015_06