2,6-Dichloroaniline → [4-(4-Benzyl-morpholin-2-yl)-phenyl]-(2,6-dichloro-phenyl)-amine

HRID 571776노트

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HRID 571776 반응식
C1C=CC(P(C2C(C3C(P(C4C=CC=CC=4)C4C=CC=CC=4)=CC=C4C=3C=CC=C4)=C3C(C=CC=C3)=CC=2)C2C=CC=CC=2)=CC=1.[CH2:47]([N:54]1[CH2:59][CH2:58][O:57][CH:56]([C:60]2[CH:65]=[CH:64][C:63](Br)=[CH:62][CH:61]=2)[CH2:55]1)[C:48]1[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=1.[Cl:67][C:68]1[CH:74]=[CH:73][CH:72]=[C:71]([Cl:75])[C:69]=1[NH2:70].CC([O-])(C)C.[Na+]>C1(C)C=CC=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[CH2:47]([N:54]1[CH2:59][CH2:58][O:57][CH:56]([C:60]2[CH:65]=[CH:64][C:63]([NH:70][C:69]3[C:68]([Cl:67])=[CH:74][CH:73]=[CH:72][C:71]=3[Cl:75])=[CH:62][CH:61]=2)[CH2:55]1)[C:48]1[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=1

참가 물질

7

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온도
100 °C

실험 절차

To a solution of BINAP (112.45 mg; 0.18 mmol) in degassed toluene (20 mL) was added 4-benzyl-2-(4-bromo-phenyl)-morpholine (1.00 g; 3.01 mmol), 2,6-dichloroaniline (0.49 g; 3.01 mmol), Pd2(dba)3 (55.12 mg; 0.06 mmol) and NaOtBu (0.29 g; 3.01 mmol). The resulting mixture was heated at 100° C. for 18 h. After cooling to RT the resulting mixture was filtered over kieselguhr, rinsed with CH2Cl2, and concentrated in vacuo. The residue was purified by column chromatography (Et2O:hexanes 1:3) to afford [4-(4-benzyl-morpholin-2-yl)-phenyl]-(2,6-dichloro-phenyl)-amine (0.73 g).

후처리

  1. temperatureAfter cooling to RT the resulting mixture
  2. filtrationwas filtered over kieselguhr
  3. washrinsed with CH2Cl2
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by column chromatography (Et2O:hexanes 1:3)

출처 및 근거

ORD 기록
ord-5319c3ecfdbd49ef8842eff46fc644a6
출처 데이터셋
uspto-grants-2015_05
특허 번호
US09029371B2

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