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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173624Generated: November 1, 2026

5-(chloromethyl)-1-methyl-1H-1,2,3,4-tetrazole → 5-tert-Butyl-3-(1-methyl-1H-tetrazol-5-ylmethyl)-7-(3,3,4,4-tetrafluoro-pyrrolidin-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine

https://huagongshe.com/reaction/2173624

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(chloromethyl)-1-methyl-1H-1,2,3,4-tetrazoleHCID 12205086—
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—
Product5-tert-Butyl-3-(1-methyl-1H-tetrazol-5-ylmethyl)-7-(3,3,4,4-tetrafluoro-pyrrolidin-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 86683350—

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 5-(chloromethyl)-1-methyl-1H-tetrazole and isolated as yellow solid. MS(m/e): 415.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056866B2
Source datasetuspto-grants-2015_06
ORD IDord-47905cf62a3548888389284529016719
Source noteuspto-grants-2015_06