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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173520Generated: October 31, 2026

(S)-(+)-2-(Methoxymethyl)pyrrolidine → 5-tert-Butyl-3-(2-chloro-benzyl)-7-((S)-2-methoxymethyl-pyrrolidin-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine

https://huagongshe.com/reaction/2173520

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(+)-2-(Methoxymethyl)pyrrolidineHCID 671217—
Reactant5-tert-Butyl-3-(2-chloro-benzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 1433953—
Reactant5-tert-butyl-7-chloro-3-(2-chlorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 86683284—
Product5-tert-Butyl-3-(2-chloro-benzyl)-7-((S)-2-methoxymethyl-pyrrolidin-1-yl)-3H-[1,2,3]triazolo[4,5-d]pyrimidineHCID 71558049—

Reaction Steps

In analogy to the procedure described for the synthesis of 5-tert-butyl-3-(2-chloro-benzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidine (example 1, step c), the title compound was prepared from 5-tert-butyl-7-chloro-3-(2-chlorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine and (S)-2-(methoxymethyl)pyrrolidine and isolated as light-yellow gum (12.0 mg, 61%). MS(m/e): 415.4 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056866B2
Source datasetuspto-grants-2015_06
ORD IDord-4208ea2eac8a4d63bd39b746f235c818
Source noteuspto-grants-2015_06