3-Nitro-6-phenylsulfanyl-imidazo[1,2-a]pyridine → HCID 53813641, 화합물

HRID 1732477노트

반응식

HRID 1732477 반응식
[N+:1]([C:4]1[N:8]2[CH:9]=[C:10]([S:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[CH:11]=[CH:12][C:7]2=[N:6][CH:5]=1)([O-])=O.[H][H]>[Pd].O1CCOCC1>[NH2:1][C:4]1[N:8]2[CH:9]=[C:10]([S:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[CH:11]=[CH:12][C:7]2=[N:6][CH:5]=1

참가 물질

5

반응물 2

HCID 541282433-Nitro-6-phenylsulfanyl-imidazo[1,2-a]pyridineHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 53813641HCID 53813641, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 312751,4-Dioxane용매

실험 절차

A solution of 0.542 gm. (0.002 mole) of 3-nitro-6-phenylthioimidazo [1,2-a] pyridine in 20 ml. of dioxane is reduced at 40 psi. under a hydrogen atmosphere with 0.500 g. of 5% palladium on carbon as catalyst. When the uptake of hydrogen is complete, the catalyst is removed by filtration. The filtrate is evaporated in vacuo to yield 3-amino-6-phenylthioimidazo [1,2-a] pyridine.

후처리

  1. customthe catalyst is removed by filtration
  2. customThe filtrate is evaporated in vacuo

출처 및 근거

ORD 기록
ord-c4c0ffac28b4472aabeb70231a6e7b4a
출처 데이터셋
uspto-grants-1980_12
특허 번호
US04237300

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