Iodine → 2-Iodo-5-methyl-4-nitroaniline

HRID 506179

반응식

HRID 506179 반응식
[CH3:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[N+:9]([O-:11])=[O:10])[NH2:5].[I:12]I>S([O-])([O-])(=O)=O.[Ag+2]>[I:12][C:6]1[CH:7]=[C:8]([N+:9]([O-:11])=[O:10])[C:2]([CH3:1])=[CH:3][C:4]=1[NH2:5]

참가 물질

4

반응물 2

HCID 807IodineHCID 118984-Nitro-m-toluidine

생성물 1

HCID 581212432-Iodo-5-methyl-4-nitroaniline

시약·촉매·용매 1

HCID 178418844HCID 178418844, 화합물촉매

실험 절차

3-Methyl-4-nitroaniline was treated with iodine and silver sulfate to give 2-iodo-5-methyl-4-nitroaniline. Treatment of the nitroaniline with 2-(trimethylsilyl)acetylene under the typical Sonogashira conditions gave 5-methyl-4-nitro-2-[(trimethylsilyl)ethynyl]aniline, which was treated with a base in an aqueous methanolic solution to give 2-ethynyl-5-methyl-4-nitroaniline. A subsequent base-induced cyclization at an elevated temperature gave 5-nitro-6-methylindole, which was treated under a high pressure hydrogenation condition to provide 5-amino-6-methylindole.

출처 및 근거

ORD 기록
ord-187d4a186cf84ac596d6a843501fc9bd
출처 데이터셋
uspto-grants-2010_08
특허 번호
US07781591B2

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