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Sodium Hydroxide → 1-[(6-Bromopyridin-3-yl)methyl]-4-ethylpiperazine

HRID 2264359
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반응식

HRID 2264359 반응식
[CH2:1]([N:3]1[CH2:8][CH2:7][NH:6][CH2:5][CH2:4]1)[CH3:2].[Br:9][C:10]1[N:15]=[CH:14][C:13]([CH:16]=O)=[CH:12][CH:11]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].[OH-].[Na+]>C(Cl)Cl>[Br:9][C:10]1[N:15]=[CH:14][C:13]([CH2:16][N:6]2[CH2:7][CH2:8][N:3]([CH2:1][CH3:2])[CH2:4][CH2:5]2)=[CH:12][CH:11]=1
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참가 물질

6

반응물 4

HCID 14798Sodium HydroxideHCID 791961-EthylpiperazineHCID 5049666Sodium triacetoxyborohydrideHCID 117692346-Bromo-3-pyridinecarboxaldehyde

생성물 1

HCID 866428861-[(6-Bromopyridin-3-yl)methyl]-4-ethylpiperazine

시약·촉매·용매 1

HCID 6344Dichloromethane용매
2회

실험 절차

Add neat 1-ethylpiperazine (221.44 mL) to a mixture of 6-bromo-pyridine-3-carbaldehyde (300 g) and DCM (5000 mL). Then, add sodium triacetoxyborohydride (372.09 g) in portions and stir at RT for 12 h. Add DCM (1000 mL) and aqueous solution of sodium hydroxide 2 N (1500 mL). Separate the layers and extract twice the aqueous layer with DCM (600 mL). Combine the organic layers and remove the solvent under vacuum, add EA and evaporate to afford 451.3 g of the title compound. MS (ES+): m/z=285 (M+H)+.

후처리

  1. customSeparate the layers
  2. extractionextract twice the aqueous layer with DCM (600 mL)
  3. customCombine the organic layers and remove the solvent under vacuum
  4. additionadd EA
  5. customevaporate

출처 및 근거

ORD 기록
ord-6dbbec81435b4a2383206b4611f3a310
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07855211B2

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