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Sodium ethoxide → HCID 117966492, 화합물

HRID 931128
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HRID 931128 반응식
[C:1]([C:3]1[CH:4]=[C:5]([S:9]([NH:12][CH3:13])(=[O:11])=[O:10])[CH:6]=[N:7][CH:8]=1)#[N:2].[O-:14][CH2:15][CH3:16].[Na+]>C(O)C>[CH3:13][NH:12][S:9]([C:5]1[CH:6]=[N:7][CH:8]=[C:3]([CH:4]=1)[C:1](=[NH:2])[O:14][CH2:15][CH3:16])(=[O:11])=[O:10]
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참가 물질

4

반응물 2

HCID 2723922Sodium ethoxideHCID 89854217HCID 89854217, 화합물

생성물 1

HCID 117966492HCID 117966492, 화합물수율 98.7%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 5-cyano-N-methylpyridine-3-sulfonamide (0.1 g, 0.5 mmol) in ethanol was added sodium ethoxide (0.03 g, 0.55 mmol). After 2 h, the mixture was concentrated under reduced pressure. The residue was partitioned between ethyl acetate and water. The organic layer was concentrated under reduced pressure to afford ethyl 5-(N-methylsulfamoyl)nicotinimidate (120 mg) as an off-white solid. The material was used without further purification. MS (ES+APCI) 244.0; LCMS retention time: 3.047 min (Method I).

후처리

  1. concentrationthe mixture was concentrated under reduced pressure
  2. customThe residue was partitioned between ethyl acetate and water
  3. concentrationThe organic layer was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e987897b24a049ceb51b7ca4a0a6b1d0
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09296745B2

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