HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905684Generated: November 1, 2026
HCID 67388691, compound → HCID 67388514, compound
https://huagongshe.com/reaction/905684
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 67388691 | HCID 67388691 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 67388514 | HCID 67388514 | 48.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012959B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-a266869ac1e94a41aa10e3bbd7053733 |
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| Source note | uspto-grants-2011_09 |
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