Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179032Generated: October 29, 2026

5-(Chloromethyl)-3-methyl-1,2,4-oxadiazole → HCID 71576596, compound

https://huagongshe.com/reaction/2179032

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Chloromethyl)-3-methyl-1,2,4-oxadiazoleHCID 12774825—
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—
ProductHCID 71576596HCID 71576596—

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 5-(chloromethyl)-3-methyl-1,2,4-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-7d20733e192248c4b448e76d101555bc
Source noteuspto-grants-2015_06