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Methanol → 4-(1,3-Benzothiazol-2-yl)-3-[2-(dimethylamino)ethoxy]aniline

HRID 339505
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HRID 339505 반응식
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:21]=[CH:20][C:19]([N+:22]([O-])=O)=[CH:18][C:11]=1[O:12][CH2:13][CH2:14][N:15]([CH3:17])[CH3:16].O.O.[Sn](Cl)Cl.CO>CCO>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:21]=[CH:20][C:19]([NH2:22])=[CH:18][C:11]=1[O:12][CH2:13][CH2:14][N:15]([CH3:17])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 61436Stannous chloride dihydrateHCID 673122622-[2-(1,3-benzothiazol-2-yl)-5-nitrophenoxy]-N,N-dimethylethanamine

생성물 1

HCID 672366574-(1,3-Benzothiazol-2-yl)-3-[2-(dimethylamino)ethoxy]aniline수율 76%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Prepared as described in the Nitro Reduction section using 2-[2-(1,3-benzothiazol-2-yl)-5-nitrophenoxy]-N,N-dimethylethanamine (0.073 g, 0.21 mmol) and tin (II) dichloride dihydrate (0.38 g, 1.7 mmol) in EtOH (7 ml) to give the title compound (0.05 g, 75%) as a cream-coloured solid after work-up and flash chromatography (MeOH).

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후처리

  1. customPrepared

출처 및 근거

ORD 기록
ord-f7d3c7909bc745f19c42e2bf41902b4c
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895313B2

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