2-(Methylamino)ethanol → HCID 178484648, 화합물

HRID 1620675노트

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HRID 1620675 반응식
Cl.[F:2][C:3]([F:34])([F:33])[C:4]1[CH:28]=[C:27]([C:29]([F:32])([F:31])[F:30])[CH:26]=[CH:25][C:5]=1[CH2:6][N:7]1[CH2:12][CH2:11][CH:10](/[CH:13]=[C:14]2/C(NCC(O)=O)=[N:16][C:17](=[O:19])[S:18]/2)[CH2:9][CH2:8]1.C(N(C(C)C)C(C)C)C.[CH3:44][NH:45][CH2:46][CH2:47][OH:48].F[P-](F)(F)(F)(F)F.C(C(=NO[C+:66](N(C)C)[N:67]1CC[O:70][CH2:69][CH2:68]1)C(OCC)=O)#N>CN(C=O)C.O>[F:34][C:3]([F:2])([F:33])[C:4]1[CH:28]=[C:27]([C:29]([F:30])([F:31])[F:32])[CH:26]=[CH:25][C:5]=1[CH2:6][N:7]1[CH2:8][CH2:9][CH:10](/[CH:13]=[C:14]2/[C:44]([NH:45][CH2:46][C:47]([N:67]([CH2:68][CH2:69][OH:70])[CH3:66])=[O:48])=[N:16][C:17](=[O:19])[S:18]/2)[CH2:11][CH2:12]1

참가 물질

7

실험 절차

To a solution of N-[(5Z)-5-({1-[2,4-bis(trifluoromethyl)benzyl]piperidin-4-yl}methylidene)-2-oxo-2,5-dihydro-1,3-thiazol-4-yl]glycine hydrochloride (500 mg), N-ethyl-N-(1-methylethyl)propan-2-amine (0.49 mL) and 2-(methylamino)ethanol (0.23 mL) in DMF (5 mL) was added (1-cyano-2-ethoxy-2-oxoethylideneaminooxy)dimethylamino-morpholino-carbenium hexafluorophosphate (403 mg), and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (NH, methanol/ethyl acetate) to give the title compound (35 mg).

후처리

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe extract was washed with water and saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customthe solvent was evaporated under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (NH, methanol/ethyl acetate)

출처 및 근거

ORD 기록
ord-b78699453d22417e93cef5ce1f78f826
출처 데이터셋
uspto-grants-2014_07
특허 번호
US08772277B2

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