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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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7-methyl-6-nitro-1H-indole → 7-methyl-1H-indol-6-amine

HRID 1275656
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HRID 1275656 반응식
[CH3:1][C:2]1[C:3]([N+:11]([O-])=O)=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][CH:8]=[CH:7]2>[Pd].C(O)C>[NH2:11][C:3]1[C:2]([CH3:1])=[C:10]2[C:6]([CH:7]=[CH:8][NH:9]2)=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 158963777-methyl-6-nitro-1H-indole

생성물 1

HCID 158963787-methyl-1H-indol-6-amine수율 76.5%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A degassed suspension of 7-methyl-6-nitroindole (1.5 g, 8.5 mmol) and catalytic 10% palladium on carbon in ethanol (75 mL) is placed under an atmosphere of hydrogen at 50 p.s.i. for 7 hours. The reaction mixture is filtered through Celite and the mixture concentrated by rotary evaporation. The crude residue is purified via silica gel column chromatography using 20% isopropanol/hexanes as the eluting solvent. The product containing fractions are combined and the solvents removed by rotary evaporation to yield 0.95 g of 6-amino-7-methylindole as a light brown solid (76% yield).

후처리

  1. filtrationThe reaction mixture is filtered through Celite
  2. concentrationthe mixture concentrated by rotary evaporation
  3. customThe crude residue is purified via silica gel column chromatography
  4. additionThe product containing fractions
  5. customthe solvents removed by rotary evaporation

출처 및 근거

ORD 기록
ord-d2a03392bdb94c01a270bc30d39bf796
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06162818

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