Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | HCID 58289931 | HCID 58289931 | — |
| Reactant | HCID 58455539 | HCID 58455539 | — |
| Product | HCID 46235832 | HCID 46235832 | — |
Reaction Steps
30 mg of the 7-chloro-3-(2,4-dichloropyridin-3-yl)-4-imino-1-methyl-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one obtained in Production Example 2, and 16 mg of TSOH monohydrate were added to a 5-ml n-butanol solution containing 20 mg of 4-{2-[(dimethylamino)methyl]morpholin-4-yl}aniline, and the mixture was heat stirred for 15 minutes at 100° C. The reaction mixture was concentrated under reduced pressure, and purified by basic column chromatography. As a result, 27 mg of a white solid was obtained as a subject compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507505B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-c85575c27c8a44729cbc3038f8bede05 |
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| Source note | uspto-grants-2013_08 |
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