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Phosphorus oxychloride → 2-(5-Amino-1,3,4-thiadiazol-2-yl)-2-methylpropanenitrile

HRID 538640
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HRID 538640 반응식
[NH2:1][NH:2][C:3]([NH2:5])=[S:4].[C:6]([C:8]([CH3:13])([CH3:12])[C:9](O)=O)#[N:7].O=P(Cl)(Cl)Cl>O1CCOCC1.Cl.C(Cl)Cl>[NH2:5][C:3]1[S:4][C:9]([C:8]([CH3:13])([CH3:12])[C:6]#[N:7])=[N:1][N:2]=1
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참가 물질

7

반응물 3

HCID 24813Phosphorus oxychlorideHCID 2723789ThiosemicarbazideHCID 113670912-Cyano-2-methylpropanoic acid

생성물 1

HCID 1176509032-(5-Amino-1,3,4-thiadiazol-2-yl)-2-methylpropanenitrile수율 32.7%

시약·촉매·용매 3

HCID 313Hydrochloric Acid용매HCID 6344
Dichloromethane
용매
HCID 312751,4-Dioxane용매

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온도
90 °C

실험 절차

300 mg (3.29 mmol) of thiosemicarbazide and 370 mg (3.27 mmol) of 2-Cyano-2-methylpropanoic acid are dissolved in dioxane (10.0 mL) and heated to 90° C. 300 μL (3.29 mmol) of POCl3 are added dropwise. The reaction is stirred at 90° C. for 1 h, cooled to RT and diluted with 1 N aq. HCl and DCM. The aq. layer is separated, 4 N aq. NaOH is added to reach pH 8 and then extracted with DCM. Then combined organic layer is washed with brine and dried. The solvent is removed under reduced pressure to afford 180 mg of 2-(5-amino[1,3,4]thiadiazol-2-yl)-2-methyl-propionitrile. Yield: 32%; ESI-MS: 169 [M+H]+; HPLC (Rt): 0.24 min (method B)

후처리

  1. temperaturecooled to RT
  2. customThe aq. layer is separated
  3. addition4 N aq. NaOH is added
  4. extractionextracted with DCM
  5. washThen combined organic layer is washed with brine
  6. customdried
  7. customThe solvent is removed under reduced pressure

출처 및 근거

ORD 기록
ord-53f5f61f81694070a76c07d7f6535c2a
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08865744B1

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