Triethylamine → HCID 67214572, 화합물

HRID 1375597노트

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HRID 1375597 반응식
C(OP(C#[N:10])(=O)OCC)C.[N:11]1[CH:16]=[CH:15][CH:14]=[C:13]([C:17]2[CH:22]=[CH:21][N:20]=[C:19]([NH:23][C:24]3[CH:25]=[C:26]([CH:30]=[CH:31][CH:32]=3)[C:27]([OH:29])=O)[N:18]=2)[CH:12]=1.[CH3:33][N:34]1[CH2:39][CH2:38][N:37]([CH2:40]C2C=CC(N)=CC=2)[CH2:36][CH2:35]1.C(N(CC)CC)C.C(=O)([O-])O.[Na+]>CN(C)C=O.O>[N:11]1[CH:16]=[CH:15][CH:14]=[C:13]([C:17]2[CH:22]=[CH:21][N:20]=[C:19]([NH:23][C:24]3[CH:25]=[C:26]([CH:30]=[CH:31][CH:32]=3)[C:27]([NH:10][CH2:40][N:37]3[CH2:36][CH2:35][N:34]([CH3:33])[CH2:39][CH2:38]3)=[O:29])[N:18]=2)[CH:12]=1

참가 물질

8

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온도
60 °C

실험 절차

Diethylcyanophosphonate (Aldrich, Buchs, Switzerland; 0.50 mL, 3.0 mmol) is added to a stirred mixture of 3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-benzoic acid (438 mg, 1.5 mmol), 4-[(4-methyl-1-piperazinyl)methyl]benzeneamine (308 mg, 1.5 mmol) and triethylamine (840 μL, 3.0 mmol) in 10 mL N,N-dimethylformamide at 10° C. After stirring for 12 hours at 60° C., the mixture is treated with an aqueous solution of sodium hydrogen carbonate and extracted three times with ethyl acetate. The combined extracts are washed with water, and the solvent is evaporated off under reduced pressure to give a residue. The residue is resuspended in water and filtered to afford the crude product which is recrystallised from tetrahydrofuran-ethyl acetate to give N-[3-[[4-(3-Pyridinyl)-2-pyrimidinyl]amino]-N-[(4-methyl-1-piperazinyl)-methyl]benzamide as a crystalline solid, m.p. 220–224° C.

후처리

  1. extractionextracted three times with ethyl acetate
  2. washThe combined extracts are washed with water
  3. customthe solvent is evaporated off under reduced pressure
  4. customto give a residue
  5. filtrationfiltered
  6. customto afford the crude product which
  7. customis recrystallised from tetrahydrofuran-ethyl acetate

출처 및 근거

ORD 기록
ord-57c2a69b6f2744c5be062ea588287333
출처 데이터셋
uspto-grants-2007_01
특허 번호
US07169791B2

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