Water → 3-ethenyl-6,7-dihydro-5H-pyrano[2,3-c]pyridazine

HRID 656955노트

반응식

HRID 656955 반응식
FC(F)(F)S(O[C:7]1[N:12]=[N:11][C:10]2[O:13][CH2:14][CH2:15][CH2:16][C:9]=2[CH:8]=1)(=O)=O.C(=O)([O-])[O-].[K+].[K+].O.CO[CH2:28][CH2:29]OC>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH:28]([C:7]1[N:12]=[N:11][C:10]2[O:13][CH2:14][CH2:15][CH2:16][C:9]=2[CH:8]=1)=[CH2:29]

참가 물질

6

실험 절차

Argon was bubbled for 15 minutes through a solution of 6,7-dihydro-5H-pyrano[2,3-c]pyridazin-3-yl trifluoromethanesulfonate (228 mg, 0.8 mmol) in 1,2-dimethoxyethane (6.5 ml). Tetrakis(triphenylphosphine)palladium(0) (50 mg, 0.0475 mmol) was added and the solution stirred for 20 minutes under argon. The mixture was then treated with potassium carbonate (111 mg, 0.8 mmol), water (1.9 ml) and triethenylboroxin pyridine complex (180 mg, 0.75 mmol). After stirring for 2 hours at 80° C., the mixture was cooled and partitioned between DCM and saturated aqueous sodium bicarbonate solution. Layers were separated and the aqueous was extracted twice with 20% MeOH/DCM. The combined organic solution was dried over magnesium sulfate, evaporated and the residue chromatographed on silica, eluting with ethyl acetate to give the product as a white solid (100 mg, 77%).

후처리

  1. stirringAfter stirring for 2 hours at 80° C.
  2. temperaturethe mixture was cooled
  3. custompartitioned between DCM and saturated aqueous sodium bicarbonate solution
  4. customLayers were separated
  5. extractionthe aqueous was extracted twice with 20% MeOH/DCM
  6. dry with materialThe combined organic solution was dried over magnesium sulfate
  7. customevaporated
  8. customthe residue chromatographed on silica
  9. washeluting with ethyl acetate

출처 및 근거

ORD 기록
ord-9b03312b503949f799295c6341ec4c12
출처 데이터셋
uspto-grants-2011_12
특허 번호
US08071592B2

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