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Ammonium Chloride → 4-(Thiazolo[4,5-c]pyridin-2-yl)benzenamine

HRID 416626
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인쇄 미리보기

반응식

HRID 416626 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[S:11][C:12]3[CH:17]=[CH:16][N:15]=[CH:14][C:13]=3[N:18]=2)=[CH:6][CH:5]=1)([O-])=O.[NH4+].[Cl-]>CO.O.[Fe]>[S:11]1[C:12]2[CH:17]=[CH:16][N:15]=[CH:14][C:13]=2[N:18]=[C:10]1[C:7]1[CH:6]=[CH:5][C:4]([NH2:1])=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 25517Ammonium ChlorideHCID 217706482-(4-Nitrophenyl)thiazolo[4,5-c]pyridine

생성물 1

HCID 217706524-(Thiazolo[4,5-c]pyridin-2-yl)benzenamine수율 60.3%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 22242641Methanol--water (1/1)용매

실험 절차

2-(4-nitrophenyl)thiazolo[4,5-c]pyridine (2.57 g, 0.01 mol), iron powder (2.8 g, 0.05 mmol) and NH4Cl (4.32 g, 0.08 mol) were refluxed in CH3OH/H2O (4:1, 200 mL) for 6 h. The mixture was filtered and the filtrate was evaporated in vacuo. The residue was washed with water (30 ml) to give 4-(thiazolo[4,5-c]pyridin-2-yl)benzenamine as a white solid (1.37 g, Yield: 60%).

후처리

  1. filtrationThe mixture was filtered
  2. customthe filtrate was evaporated in vacuo
  3. washThe residue was washed with water (30 ml)

출처 및 근거

ORD 기록
ord-f192bbbcf3254c19995132564db99333
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08088928B2

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