Water → HCID 57500672, 화합물

HRID 604373노트

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HRID 604373 반응식
Br[C:2]1[S:6][CH:5]=[N:4][C:3]=1[C:7]([O:9]C)=O.Cl.N[C:13]1[C:18]([C:19]([O:21][CH3:22])=[O:20])=[CH:17][CH:16]=[CH:15][C:14]=1B(O)O.C([O-])(=O)C.[Na+].O.C[N:33](C=O)C>C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[O:9]=[C:7]1[C:3]2[N:4]=[CH:5][S:6][C:2]=2[C:15]2[CH:16]=[CH:17][C:18]([C:19]([O:21][CH3:22])=[O:20])=[CH:13][C:14]=2[NH:33]1

참가 물질

7

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온도
120 °C

실험 절차

In a microwave vessel, methyl 5-bromothiazole-4-carboxylate (1.0 eq, 97 mg, 0.44 mmol), 2-amino-3-methoxycarbonyl phenyl boronic acid HCl (1.1 eq, 111 mg, 0.48 mmol), sodium acetate (3.0 eq, 107 mg, 1.31 mmol) and PdCl2(dppf) (0.05 eq, 11 mg, 0.022 mmol) were mixed together in anhydrous DMF (1 ml). The mixture was heated in a microwave oven at 120° C. for 10 nm. Water was added and the material extracted with CH2Cl2. The combined extracts were washed with brine, dried over Na2SO4 and the solvents removed by evaporation. The material was dissolved in a mixture of CH2Cl2 and MeOH and the solution filtered through a pad of celite. Evaporation of the volatiles afforded crude methyl 4-oxo-4,5-dihydrothiazolo[4,5-c]quinoline-7-carboxylate as a black solid (44 mg, 39% yield). A small part of the compound was subjected to preparative HPLC for analytical purpose. LCMS (ES): 95% pure, m/z 261 [M+1]+.

후처리

  1. extractionthe material extracted with CH2Cl2
  2. washThe combined extracts were washed with brine
  3. dry with materialdried over Na2SO4
  4. customthe solvents removed by evaporation
  5. dissolutionThe material was dissolved in a mixture of CH2Cl2 and MeOH
  6. filtrationthe solution filtered through a pad of celite
  7. customEvaporation of the volatiles

출처 및 근거

ORD 기록
ord-a86e31b96d45459dbe0fbe3cf463c901
출처 데이터셋
uspto-grants-2011_03
특허 번호
US07910600B2

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