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Dimethylformamide → Methyl 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carboxylate

HRID 1604648
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인쇄 미리보기

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HRID 1604648 반응식
[C]=O.FC(F)(F)S(O[C:9]1[CH:10]=[CH:11][C:12]2[O:16][C:15]([C:17]3[S:18][CH:19]=[C:20]([C:22]([CH3:25])([CH3:24])[CH3:23])[N:21]=3)=[CH:14][C:13]=2[CH:26]=1)(=O)=O.C1(OP(CCCP([O:57][C:58]2C=CC=CC=2)(OC2C=CC=CC=2)=O)(OC2C=CC=CC=2)=O)C=CC=CC=1.C(N(CC)CC)C.CN(C)[CH:73]=[O:74]>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.CO>[C:22]([C:20]1[N:21]=[C:17]([C:15]2[O:16][C:12]3[CH:11]=[CH:10][C:9]([C:73]([O:57][CH3:58])=[O:74])=[CH:26][C:13]=3[CH:14]=2)[S:18][CH:19]=1)([CH3:25])([CH3:24])[CH3:23]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 6228DimethylformamideHCID 8471TriethylamineHCID 196036842-(4-Tert-butylthiazol-2-yl)benzofuran-5-yl trifluoromethanesulfonateHCID 538511551,3-Bis(diphenylphosphono)propaneHCID 178418416HCID 178418416, 화합물

생성물 1

HCID 19603836Methyl 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carboxylate

시약·촉매·용매 2

HCID 167845palladium(II) acetate촉매HCID 887Methanol용매

반응 조건

온도
70 °C

실험 절차

Carbon monoxide was introduced by bubbling to a mixture of 2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl trifluoromethanesulfonate (6.0 g), palladium acetate (99.7 mg), 1,3-bis(diphenylphosphono)propane (183 mg, 0.44 mmol) and triethylamine (4.13 ml) in a mixed solvent of methanol (15 ml) and N,N-dimethylformamide (30 ml) at room temperature for 1 hour. The mixture was warmed to 70° C. and stirred under carbon monoxide balloon for 3 hours. The resulting mixture was filtered through celite and the residue was washed with ethyl acetate. The filtrate and washing solution was combined and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using ethyl acetate-n-hexane as eluent to give methyl 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carboxylate (3.92 g) as a colorless powder.

후처리

  1. filtrationThe resulting mixture was filtered through celite
  2. washthe residue was washed with ethyl acetate
  3. washThe filtrate and washing solution
  4. customevaporated under reduced pressure
  5. customThe residue was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-438352edabd341d88dfbc1795d420f22
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05994378

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