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(Methylthio)thioacetamide → 2-Methylthiomethyl-5-(4-nitrobenzyl)-4-propylthiazole

HRID 1613252
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반응식

HRID 1613252 반응식
Cl[CH:2]([C:13](=O)[CH2:14][CH2:15][CH3:16])[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][CH:5]=1.[CH3:18][S:19][CH2:20][C:21]([NH2:23])=[S:22]>C1CCCCC1.C(OCC)(=O)C>[CH3:18][S:19][CH2:20][C:21]1[S:22][C:2]([CH2:3][C:4]2[CH:9]=[CH:8][C:7]([N+:10]([O-:12])=[O:11])=[CH:6][CH:5]=2)=[C:13]([CH2:14][CH2:15][CH3:16])[N:23]=1
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참가 물질

4

반응물 2

HCID 19014065(Methylthio)thioacetamideHCID 19775543HCID 19775543, 화합물

생성물 1

HCID 197755752-Methylthiomethyl-5-(4-nitrobenzyl)-4-propylthiazole수율 86.8%

시약·촉매·용매 1

HCID 21867204Cyclohexane ethylacetate용매

반응 조건

온도
60 °C

실험 절차

A mixture of 5 g of 2-chloro-1-(4-nitrophenyl)-hexan-3-one (0.02 mol) and 2.6 g of (methylthio)thioacetamide (0.022 mol) is heated at 60° C. for 24 h. The reaction is followed by TLC (7/3 cyclohexane/ethyl acetate). The reaction medium is then treated according to the process of Example 45 to give 5.6 g of 2-methylthiomethyl-5-(4-nitrobenzyl)-4-propylthiazole in the form of an orange oil.

후처리

  1. additionThe reaction medium is then treated

출처 및 근거

ORD 기록
ord-70bb8c6cf0e14e1b83537ca32639d6a9
출처 데이터셋
uspto-grants-1993_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05192781

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