Dimethylformamide → 2'-Fluoro-5-(5-methyl-pyridin-2-yl)-6'-trifluoromethyl-biphenyl-3-carboxylic acid ((R)-1-methyl-2-morpholin-4-yl-ethyl)-amide
반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([C:8]([F:11])([F:10])[F:9])[C:3]=1[C:12]1[CH:17]=[C:16]([C:18]2[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][N:19]=2)[CH:15]=[C:14]([C:25]([OH:27])=O)[CH:13]=1.Cl.[O:29]1[CH2:34][CH2:33][N:32]([CH2:35][C@@H:36]([NH2:38])[CH3:37])[CH2:31][CH2:30]1.F[P-](F)(F)(F)(F)F.C[N+](C)=C(N(C)C)ON1C2N=CC=CC=2N=N1.C(N(CC)C(C)C)(C)C.CN(C)C=O>>[CH3:37][C@@H:36]([NH:38][C:25]([C:14]1[CH:13]=[C:12]([C:3]2[C:4]([C:8]([F:9])([F:10])[F:11])=[CH:5][CH:6]=[CH:7][C:2]=2[F:1])[CH:17]=[C:16]([C:18]2[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][N:19]=2)[CH:15]=1)=[O:27])[CH2:35][N:32]1[CH2:33][CH2:34][O:29][CH2:30][CH2:31]1참가 물질
6
반응물 5
생성물 1
실험 절차
A round bottom flask was charged with 2′-fluoro-5-(5-methylpyridin-2-yl)-6′-(trifluoromethyl)biphenyl-3-carboxylic acid (100.00 mg, 0.26644 mmol), (S)-1-morpholinopropan-2-amine hydrochloride (112.10 mg, 0.62047 mmol), N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (0.49150 g, 1.2926 mmol), N,N-diisopropylethylamine (0.36025 mL, 2.0682 mmol), N,N-dimethylformamide (0.882 mL, 11.4 mmol) and the reaction stirred over night at room temperature. The solvent was removed under reduced pressure and the residue purified by prep HPLC to get the compound as white solid.
후처리
- customThe solvent was removed under reduced pressure
- customthe residue purified by prep HPLC
출처 및 근거
- ORD 기록
- ord-3da76e04e2c9422b894023fc7bb91f22
- 출처 데이터셋
- uspto-grants-2015_09
- 특허 번호
- US09133122B2
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