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Potassium Carbonate → HCID 178513412, 화합물

HRID 604484
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HRID 604484 반응식
[NH2:1][C:2]1[S:3][C:4]([C:13]#[N:14])=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:6]=1.Cl.[NH2:16][OH:17].C(=O)([O-])[O-].[K+].[K+]>O.C(O)C>[NH2:1][C:2]1[S:3][C:4]([C:13]([NH:16][OH:17])=[NH:14])=[C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 443297Hydroxyamine hydrochlorideHCID 214555522-Amino-4-Phenylthiazole-5-carbonitrile

생성물 1

HCID 178513412HCID 178513412, 화합물

시약·촉매·용매 1

HCID 19096565Water ethanol용매

실험 절차

2-Amino-4-phenyl-thiazole-5-carbonitrile (0.13 g, 0.6 mmol) was suspended in 1:1 water/ethanol (v/v) (24 mL) and added hydroxylamine hydrochloride (1.47 g, 21 mmol) and potassium carbonate (1.86 g, 13 mmol). The reaction mixture was heated at reflux for 3 days, then the solvent was reduced and the aqueous phase was extracted with dichloromethane. The organic layer was washed with water and brine, and was dried over sodium sulfate. The solvent was evaporated to yield a yellow solid. Yield: 0.1 g, 66%.

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후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 3 days
  3. extractionthe aqueous phase was extracted with dichloromethane
  4. washThe organic layer was washed with water and brine
  5. dry with materialwas dried over sodium sulfate
  6. customThe solvent was evaporated
  7. customto yield a yellow solid

출처 및 근거

ORD 기록
ord-919aa211b7e649a5998c567356593ff2
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07910613B2

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