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1-Methylpiperazine → HCID 86607093, 화합물

HRID 2108874
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HRID 2108874 반응식
[Br:1][CH2:2][C:3]1[O:4][CH:5]=[C:6]([OH:10])[C:7](=[O:9])[CH:8]=1.[CH3:11][N:12]1[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]1>O1CCCC1>[BrH:1].[OH:10][C:6]1[C:7](=[O:9])[CH:8]=[C:3]([CH2:2][N:15]2[CH2:16][CH2:17][N:12]([CH3:11])[CH2:13][CH2:14]2)[O:4][CH:5]=1
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참가 물질

4

반응물 2

HCID 531671-MethylpiperazineHCID 10976603KOJIC ACID, 2-BROMOMETHYL ANALOG

생성물 1

HCID 86607093HCID 86607093, 화합물수율 83%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
75 °C

실험 절차

2-(Bromomethyl)-5-hydroxy-4H-pyran-4-one 21 (0.5 g, 2.4 mmol), 1-methylpiperazine (0.3 mL, 2.4 mmol) and tetrahydrofurane (12 mL) were charged in a 250 ml round-bottomed flask equipped with a magnetic stirrer. The reaction mixture was stirred for 2 h at 75° C. The reaction mixture was cooled and the precipitate was filtered to give after drying 5-hydroxy-2-((4-methylpiperazin-1-yl)methyl)-4H-pyran-4-one hydrobromide 23 (0.6 g, 83% yield) as a beige solid. A cesium salt was prepared by adding to Cs2CO3 (7.3 g, 22.4 mmol) in water (20 mL). The aqueous phase was washed with CH2Cl2 (200 mL), then water was evaporated at 40° C. and the cesium salt was drying under vacuum to give a white powder.

후처리

  1. customequipped with a magnetic stirrer
  2. temperatureThe reaction mixture was cooled
  3. filtrationthe precipitate was filtered
  4. customto give

출처 및 근거

ORD 기록
ord-151ff86453d94af2b49bd62468456ec6
출처 데이터셋
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07514432B2

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