関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethyl Sulfoxide | HCID 679 | — |
| 反応物 | 5'-Chloro-2'-fluoro-6-(3-fluorobenzylamino)-2,4'-bipyridine-4-carbonitrile | HCID 66936967 | — |
| 反応物 | HCID 178511674 | HCID 178511674 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | HCID 178510200 | HCID 178510200 | 80.1% |
反応手順
To a scintillation vial containing 5′-chloro-2′-fluoro-6-(3-fluorobenzylamino)-2,4′-bipyridine-4-carbonitrile (72 mg, 0.202 mmol) was added DMSO (3 ml) and trans-cyclohexane-1,4-diamine (230 mg, 2.018 mmol). The homogenous yellow reaction mixture was capped and heated to 105° C. in a oil bath for 3 hr. The reaction mixture was diluted with EtOAc and washed with sat NaHCO3, sat NaCl. The organic layer was dried Na2SO4, filtered and concentrated. The crude solid was purified by Prep HPLC and the collected fractions were combined and diluted with EtOAc and neutralized with sat NaHCO3 and then sat NaCl. The organic layer was dried over Na2SO4, filtered and concentrated to afford 2′-(trans-4-aminocyclohexylamino)-5′-chloro-6-(3-fluorobenzylamino)-2,4′-bipyridine-4-carbonitrile (73 mg, 80%). LCMS (m/z): 451.2 (MH+), retention time=0.70 min. 1H NMR (400 MHz, METHANOL-d4) d ppm 1.34-1.48 (m, 2 H) 1.50-1.64 (m, 2 H) 2.06-2.22 (m, 4 H) 3.08-3.20 (m, 1 H) 3.63-3.74 (m, 1 H) 4.61 (s, 2H) 6.81 (s, 1 H) 6.87 (s, 1 H) 6.91-6.99 (m, 1 H) 7.02 (s, 1H) 7.04-7.10 (m, 1H) 7.12-7.18 (m, 1 H) 7.25-7.36 (m, 1 H) 8.00 (s, 1 H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08415381B2 |
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| 出典データセット | uspto-grants-2013_04 |
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| ORD ID | ord-e136cd7fc61144dabd0acdbd052510ce |
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| 出典メモ | uspto-grants-2013_04 |
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