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Triethylamine → Methyl (z)-2-((((1-aminoethylidene)amino)oxy)carbonyl)isonicotinate

HRID 1892608
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인쇄 미리보기

반응식

HRID 1892608 반응식
Cl[C:2]([C:4]1[CH:5]=[C:6]([CH:11]=[CH:12][N:13]=1)[C:7]([O:9][CH3:10])=[O:8])=[O:3].[OH:14]/[N:15]=[C:16](\[NH2:18])/[CH3:17].C(N(CC)CC)C>ClCCl>[NH2:18]/[C:16](=[N:15]\[O:14][C:2]([C:4]1[CH:5]=[C:6]([CH:11]=[CH:12][N:13]=1)[C:7]([O:9][CH3:10])=[O:8])=[O:3])/[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 5487681(E)-N'-HydroxyacetimidamideHCID 45081772Methyl 2-(chlorocarbonyl)pyridine-4-carboxylate

생성물 1

HCID 87287813Methyl (z)-2-((((1-aminoethylidene)amino)oxy)carbonyl)isonicotinate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of methyl 2-(chlorocarbonyl)isonicotinate in dichloromethane (500 mL) was added (Z)—N′-hydroxyacetimidamide and triethylamine, keeping the temperature at 25-30° C. for 1 day. The reaction was concentrated in vacuo to afford (Z)-methyl 2-((1-aminoethylideneaminooxy)carbonyl)isonicotinate as a yellow solid.

후처리

  1. customat 25-30° C.
  2. customfor 1 day
  3. concentrationThe reaction was concentrated in vacuo

출처 및 근거

ORD 기록
ord-af8a40a6eebc47b8ac27041ca35e2110
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507681B2

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