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

HRID 911063
노트
인쇄 미리보기

반응식

HRID 911063 반응식
C([NH:9][C:10]([NH:12][C:13]1[CH:18]=[C:17]([O:19][CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[C:16]([Br:27])=[CH:15][N:14]=1)=[S:11])(=O)C1C=CC=CC=1.[OH-].[Na+]>C1COCC1>[CH2:20]([O:19][C:17]1[C:16]([Br:27])=[CH:15][N:14]=[C:13]([NH:12][C:10]([NH2:9])=[S:11])[CH:18]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium Hydroxide2회HCID 866347751-Benzoyl-3-(4-(benzyloxy)-5-bromopyridin-2-yl)thiourea

생성물 1

HCID 866347761-(4-(Benzyloxy)-5-bromopyridin-2-yl)thiourea수율 33.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
60 °C

실험 절차

A flask was charged with 1-benzoyl-3-(4-(benzyloxy)-5-bromopyridin-2-yl)thiourea (9.8 g, 22.2 mmol) and THF (200 mL). 6N NaOH (100 mL) and NaOH (5 g) were added. The reaction was stirred at 60° C. for 3 hours, then concentrated and filtered to give the desired product (2.54 g, 33.9% yield) as off white solid.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. concentrationconcentrated
  2. filtrationfiltered

출처 및 근거

ORD 기록
ord-0b6e172ff48a46338ae2af8944f9d1fb
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08022222B2

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