Hydrochloric Acid → Hydrochloric Acid

HRID 2115757노트

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HRID 2115757 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]=[CH:8][CH:7]=[C:6]2[O:15][C:16]1[CH:25]=[CH:24][C:23]2[C:18](=[CH:19][CH:20]=[C:21](Br)[CH:22]=2)[C:17]=1[F:27].P(C(C)(C)C)(C(C)(C)C)C(C)(C)C.[Li+].C[Si]([N-:46][Si](C)(C)C)(C)C.[ClH:51]>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].C1(C)C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]=[CH:8][CH:7]=[C:6]2[O:15][C:16]1[C:17]([F:27])=[C:18]2[C:23](=[CH:24][CH:25]=1)[CH:22]=[C:21]([NH2:46])[CH:20]=[CH:19]2.[ClH:51]

참가 물질

8

실험 절차

A mixture of 2-(6,7-dimethoxy-4-quinolyloxy)-6-bromo-1-fluoronaphthalene (Step b, 1.7 g, 4.0 mmol), Pd2(dba)3 (183 mg, 0.2 mmol, Aldrich) and P(t-Bu)3 (40 mg, 0.2 mmol, Aldrich) in a two-necked round-bottom flask was degassed under vacuum and refilled with N2. Under N2, dry toluene and LiHMDS (5 mL, 1M in THF, 5.0 mmol, Aldrich) was added to the mixture via syringe. The reaction was stirred at RT under N2 for 16 h. To the reaction was added 1N aqueous HCl (10 mL) and a yellow precipitate was collected by filtration. The solid was washed with 10 mL of water and dried in vacuo at 50° C. for 24 h to give title compound as HCl salt in the form of yellow solid. MS (ESI, pos. ion) m/z: 365 (M+1). Mass Calc'd for C21H17FN2O3: 364.12.

후처리

  1. customwas degassed under vacuum
  2. additionrefilled with N2
  3. filtrationa yellow precipitate was collected by filtration
  4. washThe solid was washed with 10 mL of water
  5. customdried in vacuo at 50° C. for 24 h

출처 및 근거

ORD 기록
ord-d39d87cf0ead4953b6bf3a6669760f51
출처 데이터셋
uspto-grants-2008_10
특허 번호
US07435823B2

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