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5-methyl-6-nitro-1H-indazole → 5-methyl-1H-indazol-6-amine

HRID 223280
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인쇄 미리보기

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HRID 223280 반응식
[CH3:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][C:10]=1[N+:11]([O-])=O)[NH:7][N:6]=[CH:5]2>C(O)C.O.N>[NH2:11][C:10]1[CH:9]=[C:8]2[C:4]([CH:5]=[N:6][NH:7]2)=[CH:3][C:2]=1[CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 126378375-methyl-6-nitro-1H-indazole2회

생성물 1

HCID 126378415-methyl-1H-indazol-6-amine수율 72.2%

시약·촉매·용매 3

HCID 222Ammonia용매HCID 702Ethanol용매HCID 962Water용매

실험 절차

8 g (45.2 mmol) of 5-methyl-6-nitro-indazole (formula 51), obtained according to E. Noelting, Ber. Dtsch. Chem. Ges. 37 (1904) 2556, are dissolved in 640 ml of 50% aqueous ethanol. A mixture of 80 g of ferrous sulphate in 400 ml of water and 80 ml of aqueous ammonia were added. The reaction mixture was refluxed for 20 hours and filtered while still hot. Removal of the ethanol and purification of the precipitated product with charcoal yielded 4.80 g (72%) of the target compound, m.p. 241°-242° C.

후처리

  1. additionwere added
  2. temperatureThe reaction mixture was refluxed for 20 hours
  3. filtrationfiltered while still hot
  4. customRemoval of the ethanol and purification of the precipitated product with charcoal

출처 및 근거

ORD 기록
ord-fb3ea4d420e54dd1a56ed33b0f20ad0c
출처 데이터셋
uspto-grants-1982_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04352931

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