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Ethanol → 3-Methyl-imidazo[2,1-b]thiazole-6-carboxylic acid ethyl ester

HRID 2164058
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반응식

HRID 2164058 반응식
P(Cl)(Cl)(Cl)(Cl)Cl.[CH3:7][C:8]1[N:9]2[CH:15]=[C:14]([C:16]([OH:18])=[O:17])[N:13]=[C:10]2[S:11][CH:12]=1.[CH2:19](O)[CH3:20]>C(Cl)Cl.O>[CH3:7][C:8]1[N:9]2[CH:15]=[C:14]([C:16]([O:18][CH2:19][CH3:20])=[O:17])[N:13]=[C:10]2[S:11][CH:12]=1
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참가 물질

6

반응물 3

HCID 702EthanolHCID 24819Phosphorus pentachlorideHCID 5028377HCID 5028377, 화합물

생성물 1

HCID 127446193-Methyl-imidazo[2,1-b]thiazole-6-carboxylic acid ethyl ester

시약·촉매·용매 2

HCID 962Water용매HCID 6344Dichloromethane용매

실험 절차

To a solution of 6.3 g of phosphorus pentachloride in 120 ml of dry methylene chloride, 5 g of 3-methyl-imidazo-(2,1-b)thiazole-6-carboxylic acid (prepared as described in Example 10) is added and the suspension obtained is refluxed for 3 hours. After vacuum evaporation of the solvent the residue obtained being 3-methyl-imidazo-(2,1-b)thiazole-6-carboxylchloride chlorohydrate is dissolved in 100 ml of abs. ethanol and the solution is refluxed for 4 hours. The solvent is removed and the residue obtained is dissolved in water. The solution obtained is neutralised to pH 7.5 to yield 5 g of 3-methyl-6-carboethoxy-imidazo-(2,1-b)thiazole; m.p. 117°-119°.

후처리

  1. customthe suspension obtained
  2. temperatureis refluxed for 3 hours
  3. customAfter vacuum evaporation of the solvent the residue
  4. customobtained
  5. dissolutionis dissolved in 100 ml of abs
  6. customThe solvent is removed
  7. customthe residue obtained
  8. customThe solution obtained

출처 및 근거

ORD 기록
ord-490a436a7d054468875099c3748ee1fa
출처 데이터셋
uspto-grants-1979_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04137320

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