Triethylamine → 2-Chloro-5-(6-methyl-pyridin-3-yl)-N-(1-p-tolyl-cyclohexylmethyl)-benzamide

HRID 456869노트

반응식

HRID 456869 반응식
[Cl:1][C:2]1[CH:10]=[CH:9][C:8]([C:11]2[CH:12]=[N:13][C:14]([CH3:17])=[CH:15][CH:16]=2)=[CH:7][C:3]=1[C:4]([OH:6])=O.ON1C2C=CC=CC=2N=N1.Cl.CN(C)CCCN=C=NCC.[C:40]1([CH3:54])[CH:45]=[CH:44][C:43]([C:46]2([CH2:52][NH2:53])[CH2:51][CH2:50][CH2:49][CH2:48][CH2:47]2)=[CH:42][CH:41]=1.C(N(CC)CC)C>CN(C)C=O.O>[Cl:1][C:2]1[CH:10]=[CH:9][C:8]([C:11]2[CH:12]=[N:13][C:14]([CH3:17])=[CH:15][CH:16]=2)=[CH:7][C:3]=1[C:4]([NH:53][CH2:52][C:46]1([C:43]2[CH:42]=[CH:41][C:40]([CH3:54])=[CH:45][CH:44]=2)[CH2:47][CH2:48][CH2:49][CH2:50][CH2:51]1)=[O:6]

참가 물질

8

실험 절차

To a solution of 2-chloro-5-(6-methyl-pyridin-3-yl)-benzoic acid (73 mg, 0.29 mmol) in N,N-dimethylformamide (4 mL) was added sequentially, stirring at room temperature for 10 minutes after each addition, 1-hydroxybenzotriazole (48 mg, 0.35 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (62 mg, 0.32 mmol), C-(1-p-tolyl-cyclohexyl)-methylamine (60 mg, 0.29 mmol) and triethylamine (31 mg, 0.31 mmol). The mixture was stirred at room temperature for 3 h. The reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by reverse phase chromatography to afford the title compound (35 mg). LCMS (m/z) 433.2 M+1.

후처리

  1. stirringThe mixture was stirred at room temperature for 3 h
  2. extractionextracted with ethyl acetate
  3. washThe combined organic extracts were washed with brine
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by reverse phase chromatography

출처 및 근거

ORD 기록
ord-8d53060b1671446182038bb3fa056a9a
출처 데이터셋
uspto-grants-2007_03
특허 번호
US07186742B2

반응 노트

불러오는 중…