HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905690Generated: October 29, 2026
Cyclohexylamine → HCID 44422660, compound
https://huagongshe.com/reaction/905690
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 67388067 | HCID 67388067 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 44422660 | HCID 44422660 | 61.6% |
Reaction Steps
A 8 ml portion of NMP solution containing 800 mg of 2-{[2-(4-hydroxyphenyl)ethyl]amino}-4-(methylsulfinyl)pyrimidine-5-carboxamide was mixed with 373 mg of cyclohexylamine and 0.87 ml of diisopropylethylamine, followed by stirring at 100° C. for 1 hour. The reaction mixture was cooled down to room temperature, and then mixed with water and extracted with ethyl acetate. The organic layer was washed with saturated brine, and then the solvent was evaporated. The resulting residue was purified by a silica gel column chromatography (chloroform:methanol), and the resulting crude crystals were recrystallized (methanol-ethyl acetate) to obtain 547 mg of 2-{[2-(4-hydroxyphenyl)ethyl]amino}-4-cyclohexylaminopyrimidine-5-carboxamide 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-2799992926eb441b9c6c41d7a039eb40 |
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| Source note | uspto-grants-2011_09 |
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