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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720658Generated: October 26, 2026

2,6-Dimethoxypyridine-3-carboxylic acid → HCID 10483696, compound

https://huagongshe.com/reaction/720658

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dimethoxypyridine-3-carboxylic acidHCID 853178—
Reactant3-Cyclopropylmethyl-8-[4-(methylamino)-benzyl]-1-(2-fluorobenzyl)-3,7-dihydropurine-2,6-dioneHCID 21891691—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTriethylamineHCID 8471—
ProductHCID 10483696HCID 10483696—

Reaction Steps

This compound was prepared by a method similar to that described in example 79 except that 2,6-dimethoxynicotinic acid (Aldrich) was used in place of N-acetyl-6-amino-2-pyridine carboxylic acid, the reaction was performed using 1 equivalent of 3-cyclopropylmethyl-8-[4-(methylamino)-benzyl]-1-(2-fluorobenzyl)-3,7-dihydropurine-2,6-dione and excess triethylamine and a catalytic amount of 4-dimethylaminopyridine were added as the final reagents to the reaction mixture. The product was purified by chromatography using silica gel eluted with 9:1 ethyl acetate/hexanes followed by crystallization from acetonitrile. MS, m/z(M+)=599.2417.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135475B2
Source datasetuspto-grants-2006_11
ORD IDord-e5afa1cbea114ad0b7e8d26af3b39261
Source noteuspto-grants-2006_11