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Trimethylaluminum → HCID 178489767, 화합물

HRID 1092133
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HRID 1092133 반응식
C[Al](C)C.[CH3:5][C@H:6]1[N:11]([CH3:12])[C@@H:10]([CH3:13])[CH2:9][N:8]([C:14]2[CH:24]=[CH:23][C:17]([C:18]([O:20]CC)=O)=[CH:16][CH:15]=2)[CH2:7]1.[CH3:25][O:26][C:27]1[CH:28]=[C:29]([CH2:35][CH2:36][C:37]2[CH:38]=[C:39]([NH2:42])[NH:40][N:41]=2)[CH:30]=[C:31]([O:33][CH3:34])[CH:32]=1>C1(C)C=CC=CC=1>[CH3:34][O:33][C:31]1[CH:30]=[C:29]([CH2:35][CH2:36][C:37]2[CH:38]=[C:39]([NH:42][C:18](=[O:20])[C:17]3[CH:16]=[CH:15][C:14]([N:8]4[CH2:9][C@H:10]([CH3:13])[N:11]([CH3:12])[C@H:6]([CH3:5])[CH2:7]4)=[CH:24][CH:23]=3)[NH:40][N:41]=2)[CH:28]=[C:27]([O:26][CH3:25])[CH:32]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 16682925TrimethylaluminumHCID 57440416ethyl 4-((3R,5S)-3,4,5-trimethylpiperazin-1-yl)benzoateHCID 178489815HCID 178489815, 화합물

생성물 1

HCID 178489767HCID 178489767, 화합물수율 33.7%

시약·촉매·용매 1

HCID 1140Toluene용매2회

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온도
60 °C

실험 절차

A 2M solution of trimethylaluminium (2.500 mL, 5.00 mmol) in toluene, was added dropwise to a stirred suspension of ethyl 4-((3R,5S)-3,4,5-trimethylpiperazin-1-yl)benzoate (0.643 g, 2 mmol) and 5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-amine (0.495 g, 2.00 mmol) in toluene (10 mL) at room temperature. The solution was then heated at 60° C. for 18 h. The reaction mixture was cooled and quenched with methanol (15 ml) and 2N hydrochloric acid (5 ml). The crude reaction mixture was purified by ion exchange chromatography on a SCX column, eluting with 7N ammonia in methanol. The appropriate fractions were evaporated to give an oil. The crude product was purified by silica column chromatography, eluting with a gradient of 0 to 10% 2.5N ammonia/MeOH in DCM. Pure fractions were evaporated to dryness to afford, on crystallisation from DCM/diethyl ether, the title compound (0.322 g, 33.7%) as a cream solid.

후처리

  1. temperatureThe reaction mixture was cooled
  2. customquenched with methanol (15 ml) and 2N hydrochloric acid (5 ml)
  3. customThe crude reaction mixture
  4. customwas purified by ion exchange chromatography on a SCX column
  5. washeluting with 7N ammonia in methanol
  6. customThe appropriate fractions were evaporated
  7. customto give an oil
  8. customThe crude product was purified by silica column chromatography
  9. washeluting with a gradient of 0 to 10% 2.5N ammonia/MeOH in DCM
  10. customPure fractions were evaporated to dryness
  11. customto afford, on crystallisation from DCM/diethyl ether

출처 및 근거

ORD 기록
ord-3c733f1e59bb414aa5d4f88bc9293621
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08129391B2

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