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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094501Generated: October 27, 2026

6-(2-Amino-6-chloro-pyrimidin-4-yloxy)-naphthalene-1-carboxylic acid → 6-(2-Amino-pyrimidin-4-yloxy)-naphthalene-1-carboxylic acid

https://huagongshe.com/reaction/1094501

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(2-Amino-6-chloro-pyrimidin-4-yloxy)-naphthalene-1-carboxylic acidHCID 86625276—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product6-(2-Amino-pyrimidin-4-yloxy)-naphthalene-1-carboxylic acidHCID 57455159—

Reaction Steps

24.4 g (77.5 mMol) 6-(2-amino-6-chloro-pyrimidin-4-yloxy)-naphthalene-1-carboxylic acid in 3.5 l THF and 100 ml Et3N are hydrogenated in the presence of 15 g Pd/C (10%; Engelhard 4505). The catalyst is filtered off and washed extensively with THF. Partial concentration of the filtrate precipitates the title compound: MS: [M+1]+=282.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133886B2
Source datasetuspto-grants-2012_03
ORD IDord-68c715efa3d64ca591aa818f4019aad2
Source noteuspto-grants-2012_03