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Ammonia → Elpetrigine

HRID 1358968
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HRID 1358968 반응식
[NH2:1][C:2]1[C:7]([C:8]2[CH:13]=[C:12]([Cl:14])[CH:11]=[C:10]([Cl:15])[C:9]=2[Cl:16])=[N:6][CH:5]=[C:4](Cl)[N:3]=1.[NH3:18]>C(O)C>[NH2:1][C:2]1[C:7]([C:8]2[CH:13]=[C:12]([Cl:14])[CH:11]=[C:10]([Cl:15])[C:9]=2[Cl:16])=[N:6][CH:5]=[C:4]([NH2:18])[N:3]=1
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참가 물질

4

반응물 2

HCID 222AmmoniaHCID 10990505HCID 10990505, 화합물

생성물 1

HCID 9926001Elpetrigine

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
180 °C

실험 절차

A suspension of 2-amino-6-chloro-3-(2,3,5-trichlorophenyl)pyrazine (0.3 g, 9.71×10−4 mole) in absolute ethanol (4 ml) and 0.880 aqueous ammonia (8.24 ml) was stirred and heated in an autoclave at 180° C. for 44 hrs The cooled mixture was evaporated in vacuo, and the residue extracted with chloroform (3×30 ml). The combined chloroform extracts were dried over anhydrous magnesium sulphate, filtered and the filtrate evaporated down in vacuo. The residue was purified by ‘flash chromatography’ using chloroform to 98:2 chloroform:methanol as the eluent. The product was triturated with 40-60° C. petroleum ether, filtered and dried in vacuo. Yield 0.155 g (56%), M.p. 178-180° C.

후처리

  1. customwas evaporated in vacuo
  2. extractionthe residue extracted with chloroform (3×30 ml)
  3. dry with materialThe combined chloroform extracts were dried over anhydrous magnesium sulphate
  4. filtrationfiltered
  5. customthe filtrate evaporated down in vacuo
  6. customThe residue was purified by ‘flash chromatography’
  7. customThe product was triturated with 40-60° C. petroleum ether
  8. filtrationfiltered
  9. customdried in vacuo

출처 및 근거

ORD 기록
ord-61690103a7a64066b531e8fb1e886290
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06599905B2

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