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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400978Generated: October 28, 2026

5-(chloromethyl)-1-methyl-1H-1,2,3,4-tetrazole → 1-(5-tert-butyl-3-((1-methyl-1H-tetrazol-5-yl)methyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)pyrrolidin-3-ol

https://huagongshe.com/reaction/400978

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(chloromethyl)-1-methyl-1H-1,2,3,4-tetrazoleHCID 12205086—
ReactantHCID 86296050HCID 86296050—
Reactant1-(3-Benzyl-5-tert-butyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)-pyrrolidin-3-olHCID 86683389—
Product1-(5-tert-butyl-3-((1-methyl-1H-tetrazol-5-yl)methyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)pyrrolidin-3-olHCID 86296047—

Reaction Steps

In analogy to the procedure described for the synthesis of (R)-1-(5-tert-butyl-3-((1-methyl-1H-tetrazol-5-yl)methyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)pyrrolidin-3-ol (example 219, step b) 1-(3-Benzyl-5-tert-butyl-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)-pyrrolidin-3-ol was hydrogenated and subsequently reacted with 5-(chloromethyl)-1-methyl-1H-tetrazole and isolated as light yellow oil. MS (m/e): 358.4 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741906B2
Source datasetuspto-grants-2014_06
ORD IDord-6ac940a224a14f4c9124e95d1ab1cb20
Source noteuspto-grants-2014_06