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Isopropyl chloroformate → 2,6-Dichloropyridine-3-carboxamide

HRID 31827
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HRID 31827 반응식
[Cl:1][C:2]1[C:7]([C:8](O)=[O:9])=[CH:6][CH:5]=[C:4]([Cl:11])[N:3]=1.C[N:13]1CCOCC1.ClC(OC(C)C)=O>ClCCl>[Cl:1][C:2]1[C:7]([C:8]([NH2:13])=[O:9])=[CH:6][CH:5]=[C:4]([Cl:11])[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7917Isopropyl chloroformateHCID 79724-MethylmorpholineHCID 8540472,6-Dichloronicotinic acid

생성물 1

HCID 221427782,6-Dichloropyridine-3-carboxamide수율 109.9%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A mixture of 2,6-dichloro-3-carboxypyridine (5.73 g, 30 mmole) and N-methylmorpholine (3.6 ml, 33 mmole) in dichloromethane (100 ml) was stirred in an ice-bath for 5 min. Isopropyl chloroformate (4.28 ml, 33 mmole) was added the reaction mixture at 0° C. The reaction mixture was stirred for 30 min and then bubbled with pure ammonia gas for 2 min. and stirred overnight at room temperature. The crude was concentrated under reduced pressure and sodium bisulfate (0.5M, 35 ml) was added with stirring. The aqueous solution was extracted with ethyl acetate (3×40 ml). The organics was washed with water and brine and dried with sodium sulfate to give yellow crude product (6.3 g, 50% pure).

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후처리

  1. stirringThe reaction mixture was stirred for 30 min
  2. custombubbled with pure ammonia gas for 2 min.
  3. stirringstirred overnight at room temperature
  4. concentrationThe crude was concentrated under reduced pressure and sodium bisulfate (0.5M, 35 ml)
  5. additionwas added
  6. stirringwith stirring
  7. extractionThe aqueous solution was extracted with ethyl acetate (3×40 ml)
  8. washThe organics was washed with water and brine
  9. dry with materialdried with sodium sulfate

출처 및 근거

ORD 기록
ord-921126856bfb47c2a39e9b6cebd883a0
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07425557B2

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