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Sodium Hydroxide → 1-(3,5,6-Trimethylpyridin-2-yl)piperazine

HRID 1804097
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반응식

HRID 1804097 반응식
Cl.[CH3:2][C:3]1[C:4]([N:11]2[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]2)=[N:5][C:6]([CH3:10])=[C:7]([CH3:9])[CH:8]=1.[OH-].[Na+]>C(OCC)(=O)C>[CH3:2][C:3]1[C:4]([N:11]2[CH2:12][CH2:13][NH:14][CH2:15][CH2:16]2)=[N:5][C:6]([CH3:10])=[C:7]([CH3:9])[CH:8]=1
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 673810521-(3,5,6-Trimethylpyridin-2-yl)piperazine hydrochloride

생성물 1

HCID 584848231-(3,5,6-Trimethylpyridin-2-yl)piperazine

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

To 1-(3,5,6-trimethylpyridin-2-yl)piperazine hydrochloride described in Preparation Example 52 were added ethyl acetate and 1N aqueous sodium hydroxide solution, and the mixture was extracted with ethyl acetate and washed with saturated brine. The solvent was evaporated to give 1-(3,5,6-trimethylpyridin-2-yl)piperazine (470 mg). By reaction and treatment in the same manner as in Preparation Example 27 and using 6-bromonicotinic acid (407 mg) and 1-(3,5,6-trimethylpyridin-2-yl)piperazine (470 mg), the title compound (620 mg) was obtained.

후처리

  1. extractionthe mixture was extracted with ethyl acetate
  2. washwashed with saturated brine
  3. customThe solvent was evaporated

출처 및 근거

ORD 기록
ord-935f41e5e92241fabc1ccf6af9f8e68a
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08354401B2

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