HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880072Generated: October 31, 2026
3-tert-Butylaniline → HCID 136041735, compound
https://huagongshe.com/reaction/880072
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-tert-Butylaniline | HCID 79334 | — |
| Reactant | 4-(4,6-Dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrate | HCID 23149411 | — |
| Reactant | Sodium (4-morpholin-4-yl-6-oxo-1,6-dihydropyrimidin-2-yl)acetate | HCID 136041844 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 136041735 | HCID 136041735 | 63.5% |
Reaction Steps
224 mg of 3-(tert-butyl)aniline are added to a solution of 261 mg of sodium [4-(morpholin-4-yl)-6-oxo-1,6-dihydropyrimidin-2-yl]acetate prepared in stage 2 of Example 1 in 10 ml of methanol. The reaction mixture is stirred at ambient temperature for 5 minutes and then 442 mg of 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholin-4-ium chloride hydrate are added. The resulting mixture is thus stirred for 30 minutes at ambient temperature. The reaction mixture is concentrated under reduced pressure. The evaporation residue is taken up with 10 ml of water and 10 ml of ethyl acetate. The resulting product is then stirred for 30 minutes. The precipitate formed is filtered off. 235 mg of N-[3-(2-methylpropan-2-yl)phenyl]-2-[4-(morpholin-4-yl)-6-oxo-1,6-dihydropyrimidin-2-yl]acetamide are thus obtained in the form of a white solid, the characteristics of which are the following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08993565B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-84820cd287714b61b94bfba9f5f7efe4 |
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| Source note | uspto-grants-2015_03 |
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