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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905684Generated: November 1, 2026

HCID 67388691, compound → HCID 67388514, compound

https://huagongshe.com/reaction/905684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67388691HCID 67388691—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 67388514HCID 6738851448.6%

Reaction Steps

A 20 ml portion of THF-methanol (2:1) mixed solution of 290 mg of 4-[(2-benzyloxy-6-fluorobenzyl)amino]-2-[(4-morpholin-4-ylphenyl)amino]pyrimidine-5-carboxamide synthesized in the same manner as in Production Example 13 was mixed with 50 mg of 10% palladium-carbon, followed by stirring for 1 hour in a hydrogen atmosphere. The reaction mixture was filtered and then mixed with 100 mg of 10% palladium-carbon, followed by stirring for 6 hours in a hydrogen atmosphere. After filtration of the reaction mixture and subsequent evaporation of the solvent, the resulting residue was purified by a silica gel column chromatography (chloroform-methanol). By recrystallizing the resulting crude crystals (THF-methanol), 117 mg of 4-[(2-hydroxy-6-fluorobenzyl)amino]-2-[(4-morpholin-4-ylphenyl)amino]pyrimidine-5-carboxamide was obtained as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012959B2
Source datasetuspto-grants-2011_09
ORD IDord-a266869ac1e94a41aa10e3bbd7053733
Source noteuspto-grants-2011_09