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Chloroacetaldehyde → HCID 486298, 화합물

HRID 1073208
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반응식

HRID 1073208 반응식
[NH2:1][C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.Cl[CH2:12][CH:13]=O>C(O)CCC>[N:1]1[CH:12]=[CH:13][N:6]2[C:5]3[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=3[S:3][C:2]=12
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참가 물질

4

반응물 2

HCID 33ChloroacetaldehydeHCID 8706Benzo(d)thiazol-2-amine

생성물 1

HCID 486298HCID 486298, 화합물

시약·촉매·용매 1

HCID 2631-Butanol용매

실험 절차

In 250 ml of n-butanol were heated 10.0 g of 2-aminobenzothiazole and 30 ml of 40% chloroacetaldehyde at 90° C. for 27 hours. After the solvent was removed (evaporated to dryness), the residue was crystallized in isopropanol-acetone to give 6.2 g of imidazo[2,1-b]benzothiazole. Subsequently, 4.0 g of the crystals were added to a mixture of 50 ml of dry dimethylformamide and 3.5 ml of phosphorus oxychloride followed by heating at 60° C. for 3 hours and at 75° C. for 6 hours. After completion of the reaction, the reaction mixture was poured onto ice water. After neutralizing with potassium carbonate, the mixture was extracted with ethyl acetate. The ethyl acetate was removed to give 2.2 g of 3-formylimidazo[2,1-b]benzothiazole. The thus obtained formyl compound, 1.3 g, was added to 20 ml of ethanol and furthermore 0.1 g of sodium borohydride was added to the mixture while stirring under ice cooling. After stirring at the same temperature for 10 minutes, the solvent was removed. The residue was treated with water and filtered to give 1.2 g of the title compound.

후처리

  1. customAfter the solvent was removed
  2. custom(evaporated to dryness)
  3. customthe residue was crystallized in isopropanol-acetone

출처 및 근거

ORD 기록
ord-7ad41aeef0ca473698b3d41cf086a3d4
출처 데이터셋
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04968708

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