HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1819429Generated: November 1, 2026
1,4-Dibromobutane → HCID 178526828, compound
https://huagongshe.com/reaction/1819429
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178511546 | HCID 178511546 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178526828 | HCID 178526828 | 25% |
Reaction Steps
To a solution of N4-[(trans-4-aminocyclohexyl)methyl]-N2-[5-chloro-2-(trifluoromethoxy)benzyl]-5-nitropyrimidine-2,4-diamine (51 mg, 0.1 mmol) in DMF (0.5 mL) was added 1,4-dibromobutane (36 μL, 0.3 mmol) and DIPEA (104 μL, 0.6 mmol). The reaction mixture was stirred at 50° C. for 24 h and then 72 h at room temperature. The reaction mixture was then partitioned between EtOAc (20 mL) and saturated NaHCO3 (less than 1 mL). The organic phase was washed with water (2×2 mL) and dried over Na2SO4. The resulting residue was purified by preparative HPLC to afford 13 mg (25%) of the title compound as a yellow oily solid, m/z 529.3 [M+1]+
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-5db81b5e018847a680bdbb0cd548b10d |
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| Source note | uspto-grants-2009_10 |
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