Triethylamine → HCID 178448747, 화합물

HRID 1931135노트

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HRID 1931135 반응식
[C:1]([C:5]1[S:9][C:8](=[NH:10])[N:7]([CH2:11][CH2:12][CH2:13][CH3:14])[N:6]=1)([CH3:4])([CH3:3])[CH3:2].O.N1(O)C2C=CC=CC=2N=N1.Cl.C(N=C=NCCCN(C)C)C.[Cl:38][C:39]1[CH:40]=[CH:41][C:42]([F:48])=[C:43]([CH:47]=1)[C:44](O)=[O:45].C(N(CC)CC)C>C1COCC1.C(OCC)(=O)C.C([O-])(O)=O.[Na+]>[C:1]([C:5]1[S:9]/[C:8](=[N:10]\[C:44](=[O:45])[C:43]2[CH:47]=[C:39]([Cl:38])[CH:40]=[CH:41][C:42]=2[F:48])/[N:7]([CH2:11][CH2:12][CH2:13][CH3:14])[N:6]=1)([CH3:4])([CH3:3])[CH3:2]

참가 물질

9

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온도
70 °C

실험 절차

To a mixture of Example 162C (250 mg, 1.17 mmol), 1H-benzo[d][1,2,3]triazol-1-ol hydrate (179 mg, 1.17 mmol), N1-((ethylimino)methylene)-N3, N3-dimethylpropane-1,3-diamine hydrochloride (225 mg, 1.17 mmol), 5-chloro-2-fluorobenzoic acid (205 mg, 1.17 mmol) in 8 mL of THF was added triethylamine (163 μL, 1.17 mmol). The mixture was heated at 70° C. for 12 hours then cooled to ambient temperature and diluted with ethyl acetate and aqueous NaHCO3. The organic extract was concentrated and the residue was purified by chromatography on SiO2 using an Analogix® Intelliflash280™ (Hex-EtOAc, 0 to 30% gradient) to give the title compound. LC/MS m/z 369 (M+H)+.

후처리

  1. temperaturethen cooled to ambient temperature
  2. extractionThe organic extract
  3. concentrationwas concentrated
  4. customthe residue was purified by chromatography on SiO2 using an Analogix® Intelliflash280™ (Hex-EtOAc, 0 to 30% gradient)

출처 및 근거

ORD 기록
ord-1130e649ff3043118421c29995fee5a3
출처 데이터셋
uspto-grants-2012_05
특허 번호
US08188135B2

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