1,4-Dioxane → Methyl 4-(6-pyridin-3-ylpyrazolo[1,5-c]pyrimidin-3-yl)thiophene-2-carboxylate

HRID 1255859노트

반응식

HRID 1255859 반응식
CC1(C)C(C)(C)OB([C:9]2[CH:10]=[C:11]([C:14]([O:16][CH3:17])=[O:15])[S:12][CH:13]=2)O1.Br[C:20]1[CH:21]=[N:22][N:23]2[CH:28]=[C:27](C3C=NC=CC=3)[CH:26]=[N:25][C:24]=12.C(=O)(O)[O-].[Na+].O1[CH2:45][CH2:44]OCC1>>[N:22]1[CH:45]=[CH:44][CH:24]=[C:20]([N:25]2[CH:26]=[CH:27][C:28]3=[C:20]([C:9]4[CH:10]=[C:11]([C:14]([O:16][CH3:17])=[O:15])[S:12][CH:13]=4)[CH:21]=[N:22][N:23]3[CH2:24]2)[CH:21]=1

참가 물질

5

반응 조건

온도
85 °C

실험 절차

A solution of methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-2-carboxylate (1.09 g, 4.1 mmol) and 3-bromo-6-pyridin-3-ylpyrazolo[1,5-a]pyrimidine (1.1 g, 4.1 mmol) in dioxane (20 mL) and 1M aqueous sodium bicarbonate (12.2 mL, 12.2 mmol) was degassed with nitrogen and treated with palladium tetrakistriphenylphosphine (0.24 g, 0.20 mmol) and heated to 85° C. for 16 hours. The reaction was cooled to room temperature and partitioned between water/methylene chloride. The organics were washed with water and brine, dried over sodium sulfate, filtered and evaporated in vacuo. Purification by flash chromatography (1-5% methanol/methylene chloride) gave methyl 4-(6-pyridin-3-ylpyrazolo[1,5-c]pyrimidin-3-yl)thiophene-2-carboxylate. LC-MS SIMS: m/z 337.1 [M+H]+.

후처리

  1. temperatureThe reaction was cooled to room temperature
  2. custompartitioned between water/methylene chloride
  3. washThe organics were washed with water and brine
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. customevaporated in vacuo
  7. customPurification by flash chromatography (1-5% methanol/methylene chloride)

출처 및 근거

ORD 기록
ord-05c14e3c721f47ba83f5e5b536ae1fe4
출처 데이터셋
uspto-grants-2013_06
특허 번호
US08461162B2

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