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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173627Generated: October 25, 2026

Oxalic acid--2-oxa-6-azaspiro(3.3)heptane (1/1) → 5-tert-Butyl-3-(4-methoxy-benzyl)-7-(2-oxa-6-aza-spiro[3.3]hept-6-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine

https://huagongshe.com/reaction/2173627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalic acid--2-oxa-6-azaspiro(3.3)heptane (1/1)HCID 53308464—
Reactant4-(5-tert-butyl-3-(4-methoxy benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)morpholineHCID 71558051—
Reactant5-tert-butyl-7-chloro-3-(4-methoxybenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 86683299—
Product5-tert-Butyl-3-(4-methoxy-benzyl)-7-(2-oxa-6-aza-spiro[3.3]hept-6-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 86683353—

Reaction Steps

In analogy to the procedure described for the synthesis of 4-(5-tert-butyl-3-(4-methoxy benzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidin-7-yl)morpholine (example 58, step c), the title compound was prepared from 5-tert-butyl-7-chloro-3-(4-methoxybenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine and 2-oxa-6-azaspiro[3.3]heptane oxalate and used without further purification in the consecutive step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056866B2
Source datasetuspto-grants-2015_06
ORD IDord-8818f5712f144633804cc787736d4c23
Source noteuspto-grants-2015_06