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Ammonium Chloride → 5,7-dimethyl-1H-pyrazolo[3,4-c]pyridine

HRID 1527297
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HRID 1527297 반응식
Br[C:2]1[N:3]=[C:4]([CH3:11])[CH:5]=[C:6]2[CH:10]=[N:9][NH:8][C:7]=12.[CH3:12][Al](C)C.[NH4+].[Cl-]>C1COCC1.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>[CH3:11][C:4]1[CH:5]=[C:6]2[CH:10]=[N:9][NH:8][C:7]2=[C:2]([CH3:12])[N:3]=1
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참가 물질

6

반응물 3

HCID 25517Ammonium ChlorideHCID 16682925TrimethylaluminumHCID 866738187-bromo-5-methyl-1H-pyrazolo[3,4-c]pyridine

생성물 1

HCID 682836325,7-dimethyl-1H-pyrazolo[3,4-c]pyridine

시약·촉매·용매 2

HCID 178418397HCID 178418397, 화합물촉매
HCID 8028
Tetrahydrofuran
용매

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온도
65 °C

실험 절차

To a vigorously stirred solution of 7-bromo-5-methyl-1H-pyrazolo[3,4-c]pyridine (3.65 g, 14.6 mmol) and Pd(PPh3)4 (845 mg, 0.73 mmol) in THF (65 mL) was added trimethylaluminum (14.6 mL, 29.3 mmol; 2 M sol. in toluene) under argon. The reaction mixture was stirred at 65° C. for 60 h, and then was cooled to RT and poured into a sat. aq. NH4Cl solution. The resulting suspension was filtered, the solid was washed with water and discarded. The filtrate and the combined washings were extracted with EtOAc (3×). The combined organics were washed with brine, then dried (Phase separator) and concentrated under reduced pressure to give 5,7-dimethyl-1H-pyrazolo[3,4-c]pyridine as a solid. MS (LC-MS): 148 [M+H]+, tR (HPLC conditions k): 0.50 min.

후처리

  1. temperaturewas cooled to RT
  2. filtrationThe resulting suspension was filtered
  3. washthe solid was washed with water
  4. extractionThe filtrate and the combined washings were extracted with EtOAc (3×)
  5. washThe combined organics were washed with brine
  6. customdried (Phase separator)
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-0411f260596045d087619d14a0e591b5
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09085555B2

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