Diisopropylethylamine → N-[(3S,5S,6R)-6-Methyl-2-oxo-5-phenyl-1-(2,2,2-trifluoroethyl)piperidin-3-yl]-2'-oxo-1',2'-dihydro-3H-spiro[1-benzofuran-2,3'-pyrrolo[2,3-b]pyridine]-5-carboxamide

HRID 931401노트

반응식

HRID 931401 반응식
F[P-](F)(F)(F)(F)F.N1(O[P+](N(C)C)(N(C)C)N(C)C)[C:12]2C=CC=C[C:11]=2N=N1.[O:28]=[C:29]1[N:37](COCC[Si](C)(C)C)[C:32]2=[N:33][CH:34]=[CH:35][CH:36]=[C:31]2[C:30]21[O:56][C:48]1=NC=[C:51]([C:53]([OH:55])=O)[CH:52]=[C:47]1[CH2:46]2.Cl.[NH2:58][C@H:59]1[CH2:64][C@@H:63]([C:65]2[CH:70]=[CH:69][CH:68]=[CH:67][CH:66]=2)[C@@H:62]([CH3:71])[N:61]([CH2:72][C:73]([F:76])([F:75])[F:74])[C:60]1=[O:77].C(N(CC)C(C)C)(C)C>CN(C=O)C>[CH3:71][C@H:62]1[N:61]([CH2:72][C:73]([F:74])([F:75])[F:76])[C:60](=[O:77])[C@@H:59]([NH:58][C:53]([C:51]2[CH:11]=[CH:12][C:48]3[O:56][C:30]4([C:31]5[C:32](=[N:33][CH:34]=[CH:35][CH:36]=5)[NH:37][C:29]4=[O:28])[CH2:46][C:47]=3[CH:52]=2)=[O:55])[CH2:64][C@H:63]1[C:65]1[CH:70]=[CH:69][CH:68]=[CH:67][CH:66]=1

참가 물질

6

실험 절차

(Benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (90 mg, 0.20 mmol) is added to a solution of 2′-oxo-1′,2′-dihydro-3H-spiro[benzofuran-2,3′-pyrrolo[2,3-b]pyridine]-5-carboxylic acid (described in Intermediate 2) (48 mg, 0.17 mmol), (3S,5S,6R)-3-amino-6-methyl-5-phenyl-1-(2,2,2-trifluoroethyl)piperidin-2-one hydrochloride (described in Intermediate 1, 54 mg, 0.17 mmol), and N,N-diisopropylethylamine (0.15 mL, 0.84 mmol) in DMF (3 mL), and the resulting mixture is stirred at ambient temperature for 3 h. The reaction mixture is then partitioned between saturated aqueous sodium bicarbonate solution (20 mL) and ethyl actetate (3×20 mL). The combined organic layers are washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue is purified by flash column chromatography on silica gel, eluting with a gradient of CH2Cl2:MeOH—100:0 to 90:10, to afford the title compound as a mixture of diastereomers.

후처리

  1. customThe reaction mixture is then partitioned between saturated aqueous sodium bicarbonate solution (20 mL) and ethyl actetate (3×20 mL)
  2. washThe combined organic layers are washed with brine
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated in vacuo
  5. customThe residue is purified by flash column chromatography on silica gel
  6. washeluting with a gradient of CH2Cl2

출처 및 근거

ORD 기록
ord-2aa00f794fa64ca7b44f3d1825f9e1bb
출처 데이터셋
uspto-grants-2016_03
특허 번호
US09296750B2

반응 노트

불러오는 중…