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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Oxalyl chloride → 5-Bromo-2-chloro-3-pyridinecarbonyl chloride

HRID 1518509
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HRID 1518509 반응식
[Br:1][C:2]1[CH:3]=[N:4][C:5]([Cl:11])=[C:6]([CH:10]=1)[C:7](O)=[O:8].C(Cl)(=O)C([Cl:15])=O>C(Cl)Cl.CN(C)C=O>[Br:1][C:2]1[CH:10]=[C:6]([C:7]([Cl:15])=[O:8])[C:5]([Cl:11])=[N:4][CH:3]=1
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참가 물질

5

반응물 2

HCID 65578Oxalyl chlorideHCID 27633425-Bromo-2-chloronicotinic acid

생성물 1

HCID 126772955-Bromo-2-chloro-3-pyridinecarbonyl chloride수율 99.4%

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 6344Dichloromethane용매

실험 절차

To a slurry of 5-bromo-2-chloronicotinic acid (2.063 g, 8.725 mmol) in methylene chloride (20 mL) was slowly added oxalyl chloride (1.11 g, 8.725 mmol) followed by the addition of dimethylformamide (5 drops). After 4H the mixture was concentrated in vacuo to provide 2.21 g of 5-bromo-2-chloropyridine-3-carbonyl chloride as a light brown solid, which was used as is in the next reaction.

후처리

  1. concentrationAfter 4H the mixture was concentrated in vacuo

출처 및 근거

ORD 기록
ord-6c60691e92624cf885feaaa13f5d2984
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08232406B2

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