HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819434Generated: November 3, 2026
Diisopropylethylamine → HCID 178450743, compound
https://huagongshe.com/reaction/1819434
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl 2,4-dibromobutyrate | HCID 5107723 | — |
| Reactant | HCID 178511544 | HCID 178511544 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178450743 | HCID 178450743 | 29% |
Reaction Steps
To a solution of N4-[(trans-4-aminocyclohexyl)methyl]-5-nitro-N2-[2-(trifluoromethoxy)benzyl]-pyrimidine-2,4-diamine (300 mg, 0.69 mmol) in DMF (3 mL) were added t-butyl 2,4-dibromobutyrate (322 μL, 1.5 mmol) and DIPEA (297 μL), 1.7 mmol). The reaction mixture was stirred at 60° C. for 9 h. The reaction mixture was then diluted with EtOAc and washed with 1M Na2CO3, water (×4) and brine. The organic phase was then dried over Na2SO4 and concentrated. The resulting residue was purified by silica gel preparative TLC using 98:2 CH2Cl2:MeOH as an eluent to afford 116 mg of 1-(trans-4-{[(5-nitro-2-{[2-(trifluoromethoxy)benzyl]amino}pyrimidin-4-yl)amino]methyl}cyclohexyl)azetidine-2-carboxylic acid tert-butyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601714B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-2a0fd2eb55be4801b8ee4b0f77394c2e |
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| Source note | uspto-grants-2009_10 |
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