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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400939Generated: October 26, 2026

2-(Chloromethyl)-5-methyl-1,3,4-oxadiazole → HCID 86683349, compound

https://huagongshe.com/reaction/400939

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Chloromethyl)-5-methyl-1,3,4-oxadiazoleHCID 3826620—
Reactant5-tert-Butyl-7-(3,3-difluoro-pyrrolidin-1-yl)-3-ethyl-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 71558205—
ReactantHCID 178441794HCID 178441794—
ProductHCID 86683349HCID 86683349—

Reaction Steps

In analogy to the procedure described for the synthesis of 5-tert-butyl-7-(3,3-difluoropyrrolidin-1-yl)-3-ethyl-3H-[1,2,3]triazolo[4,5-d]pyrimidine (example 61), 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 2-(chloromethyl)-5-methyl-1,3,4-oxadiazole and isolated as light-yellow gum. MS (m/e): 415.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741906B2
Source datasetuspto-grants-2014_06
ORD IDord-d4777018d1cb4909aca580633012a901
Source noteuspto-grants-2014_06