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4-Chlorobenzyl alcohol → HCID 14072382, 화합물

HRID 1165431
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HRID 1165431 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[C:13](=[O:14])[C:12]([Cl:15])=[C:11](Cl)[CH:10]=[N:9]2)=[N:6][CH:7]=1.[Cl:17][C:18]1[CH:25]=[CH:24][C:21]([CH2:22][OH:23])=[CH:20][CH:19]=1.[OH-].[K+]>CN(C)C=O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[C:13](=[O:14])[C:12]([Cl:15])=[C:11]([O:23][CH2:22][C:21]3[CH:24]=[CH:25][C:18]([Cl:17])=[CH:19][CH:20]=3)[CH:10]=[N:9]2)=[N:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 133974-Chlorobenzyl alcoholHCID 14797Potassium HydroxideHCID 198618124,5-Dichloro-2-(5-chloropyridin-2-yl)pyridazin-3(2H)-one

생성물 1

HCID 14072382HCID 14072382, 화합물수율 25.5%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

In 30 ml of N,N-dimethylformamide were dissolved 1.5 g (5.1 m mol) of 2-(5-chloropyridine-2-yl)-4,5-dichloropyridazinone and 0.73 g (5.1 m mol) of p-chlorobenzyl alcohol, and thereto was added 0.34 g of powdery potassium hydroxide. Then, the procedures in Synthesis Example 2 were repeated to give 500 mg of the intended compound.

후처리

  1. customThen, the procedures in Synthesis Example 2

출처 및 근거

ORD 기록
ord-31fa828a93b845c6902c96462d505b4d
출처 데이터셋
uspto-grants-1990_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04910201

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