HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712247Generated: October 30, 2026
Water → Ethyl 4-(5-bromopyrimidin-2-ylamino)-1-methylcyclohexanecarboxylate
https://huagongshe.com/reaction/712247
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Bromo-2-chloropyrimidine | HCID 606665 | — |
| Reactant | Ethyl 4-amino-1-methylcyclohexanecarboxylate | HCID 58291914 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-(5-bromopyrimidin-2-ylamino)-1-methylcyclohexanecarboxylate | HCID 66976994 | 19.3% |
Reaction Steps
To an ice-cold solution of ethyl 4-amino-1-methylcyclohexanecarboxylate (0.18 g, 0.97 mmol) in EtOH (5.0 mL) was added DIPEA (0.52 mL, 2.91 mmol) followed by the addition of 5-bromo-2-chloropyrimidine (0.185 g, 0.97 mmol). The mixture was heated to 80° C. for 6-8 h after then cooled to rt, water added and extracted with EtOAc (3×100 mL). The combined organics were washed with brine, dried over anhydrous Na2SO4, filtered and evaporated under reduced pressure. The crude residue was purified over 100-200 M silica-gel by using 4% EtOAc:hexane to obtain the desired product (0.064 g, 19%). MS: 342.01 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181234B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-242d835b2ee14af2b83f77d8d840a3d5 |
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| Source note | uspto-grants-2015_11 |
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