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Sodium Hydroxide → 1-(4-(4-Methoxybenzylthio)-5-bromopyridin-2-yl)thiourea

HRID 911056
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인쇄 미리보기

반응식

HRID 911056 반응식
[CH3:1][O:2][C:3]1[CH:29]=[CH:28][C:6]([CH2:7][S:8][C:9]2[C:14]([Br:15])=[CH:13][N:12]=[C:11]([NH:16][C:17]([NH:19]C(=O)C3C=CC=CC=3)=[S:18])[CH:10]=2)=[CH:5][CH:4]=1.[OH-].[Na+]>C1COCC1>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][S:8][C:9]2[C:14]([Br:15])=[CH:13][N:12]=[C:11]([NH:16][C:17]([NH2:19])=[S:18])[CH:10]=2)=[CH:28][CH:29]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 866347701-(4-(4-Methoxybenzylthio)-5-bromopyridin-2-yl)-3-benzoylthiourea

생성물 1

HCID 866347711-(4-(4-Methoxybenzylthio)-5-bromopyridin-2-yl)thiourea수율 79.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
65 °C

실험 절차

1-(4-(4-methoxybenzylthio)-5-bromopyridin-2-yl)-3-benzoylthiourea (8.50 g, 17.4 mmol) was suspended in THF (150 mL). NaOH (116 ml, 348 mmol) was added, and the reaction was stirred at 65° C. overnight. The solution was cooled and filtered, and the solids were washed with cold water. The solids were then triturated in EtOH and filtered to provide the desired product (5.3 g, 79% yield) as a tan solid.

후처리

  1. temperatureThe solution was cooled
  2. filtrationfiltered
  3. washthe solids were washed with cold water
  4. customThe solids were then triturated in EtOH
  5. filtrationfiltered

출처 및 근거

ORD 기록
ord-4dac2e2829574ed58bebae90fc7f772c
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08022222B2

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