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Water → 2-Methoxymethyl-4-propyl-5-(4-aminobenzyl)thiazole

HRID 1613240
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반응식

HRID 1613240 반응식
[CH3:1][O:2][CH2:3][C:4]1[S:5][C:6]([CH2:12][C:13]2[CH:18]=[CH:17][C:16]([N+:19]([O-])=O)=[CH:15][CH:14]=2)=[C:7]([CH2:9][CH2:10][CH3:11])[N:8]=1.O>CO.[Ni]>[CH3:1][O:2][CH2:3][C:4]1[S:5][C:6]([CH2:12][C:13]2[CH:14]=[CH:15][C:16]([NH2:19])=[CH:17][CH:18]=2)=[C:7]([CH2:9][CH2:10][CH3:11])[N:8]=1
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참가 물질

5

반응물 2

HCID 962WaterHCID 19775540HCID 19775540, 화합물

생성물 1

HCID 197755572-Methoxymethyl-4-propyl-5-(4-aminobenzyl)thiazole

시약·촉매·용매 2

HCID 935Nickel촉매HCID 887Methanol용매

실험 절차

0.9 of 2-methoxymethyl-4-propyl-5-(4-nitrobenzyl)thiazole in 50 ml of methanol is hydrogenated at normal pressure and room temperature in the presence of Raney nickel. After filtration of the catalyst and concentration of the filtrate, the brown oil obtained is taken up with acidified water. The aqueous phase is extracted with ether, rendered basic with dilute sodium hydroxide and extracted with ethyl acetate. The organic phase is dried and concentrated to give 0.5 g of 2-methoxymethyl-4-propyl-5-(4-aminobenzyl)thiazole in the form of an orange oil, which is used as such for the next step.

후처리

  1. filtrationAfter filtration of the catalyst and concentration of the filtrate
  2. customthe brown oil obtained
  3. extractionThe aqueous phase is extracted with ether
  4. extractionextracted with ethyl acetate
  5. customThe organic phase is dried
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-291153c75bb64ab7a281eea7dc8a7e34
출처 데이터셋
uspto-grants-1993_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05192781

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