Potassium Phosphate, Tribasic → (3-Fluoro-2'-(trifluoromethyl)-[2,4'-bipyridin]-5-yl)methanamine
반응식
Cl[C:2]1[N:7]=[CH:6][C:5]([CH2:8][NH2:9])=[CH:4][C:3]=1[F:10].[F:11][C:12]([F:23])([F:22])[C:13]1[CH:18]=[C:17](B(O)O)[CH:16]=[CH:15][N:14]=1.COC1C=CC=C(OC)C=1C1C=CC=CC=1P(C1CCCCC1)C1CCCCC1.P([O-])([O-])([O-])=O.[K+].[K+].[K+]>CC([O-])=O.CC([O-])=O.[Pd+2].CC(O)CC>[F:10][C:3]1[C:2]([C:17]2[CH:16]=[CH:15][N:14]=[C:13]([C:12]([F:23])([F:22])[F:11])[CH:18]=2)=[N:7][CH:6]=[C:5]([CH2:8][NH2:9])[CH:4]=1참가 물질
반응물 4
생성물 1
시약·촉매·용매 2
반응 조건
- 온도
- 100 °C
실험 절차
To a flask containing (6-chloro-5-fluoropyridin-3-yl)methanamine 84-1 (353 mg, 2.20 mmol), 2-(trifluoromethyl)pyridin-4-ylboronic acid 33-1 (418 mg, 2.20 mmol), Pd(OAc)2 (29 mg, 0.11 mmol), S-Phos (91 mg, 0.22 mmol) and potassium phosphate (1.40 g, 6.60 mmol) under Argon was added 2-butanol (4 mL). The mixture was stirred at 100° C. for 10 hours. After cooling to room temperature, the mixture was filtered through celite cake. The filtrate was diluted with ethyl acetate, washed with H2O and brine, dried over Na2SO4, and concentrated to dryness by rotary evaporation. The crude product was purified by silica gel flash chromatography, and eluted with 5% methanol containing ˜7N ammonia in dichloromethane to give (3-fluoro-2′-(trifluoromethyl)-2,4′-bipyridin-5-yl)methanamine 84-2 as a pale yellow solid. MS m/z 268.1 (M+1)
후처리
- temperatureAfter cooling to room temperature
- filtrationthe mixture was filtered through celite cake
- additionThe filtrate was diluted with ethyl acetate
- washwashed with H2O and brine
- dry with materialdried over Na2SO4
- concentrationconcentrated to dryness by rotary evaporation
- customThe crude product was purified by silica gel flash chromatography
- washeluted with 5% methanol containing ˜7N ammonia in dichloromethane
출처 및 근거
- ORD 기록
- ord-24692876f15b4798ab880b7f9b3e0fe1
- 출처 데이터셋
- uspto-grants-2015_11
- 특허 번호
- US09181235B2
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