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Hydrochloric Acid → HCID 71532156, 화합물

HRID 518134
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HRID 518134 반응식
Br[C:2]1[CH:6]=[CH:5][S:4][C:3]=1[CH2:7][C:8]#[N:9].[CH:10](OCC)=O.[O-]CC.[Na+].C(O)C.Cl.[NH2:23][C:24]1[CH:32]=[CH:31][C:27]([C:28]([OH:30])=[O:29])=[C:26]([OH:33])[CH:25]=1.P([O-])([O-])([O-])=O.[K+].[K+].[K+].Cl>CS(C)=O.[Cu]I.C(O)CO.O>[C:8]([C:7]1[C:3]2[S:4][CH:5]=[CH:6][C:2]=2[N:23]([C:24]2[CH:32]=[CH:31][C:27]([C:28]([OH:30])=[O:29])=[C:26]([OH:33])[CH:25]=2)[CH:10]=1)#[N:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

12

반응물 7

HCID 313Hydrochloric AcidHCID 46494-Aminosalicylic AcidHCID 8025Ethyl formateHCID 62657Potassium Phosphate, TribasicHCID 2723922Sodium ethoxideHCID 18628861209796-27-0HCID 21887872Ethanol hydrochloride

생성물 1

HCID 71532156
HCID 71532156, 화합물
수율 32%

시약·촉매·용매 4

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 174Ethylene Glycol용매HCID 679Dimethyl Sulfoxide용매2회HCID 962Water용매

실험 절차

To a solution of 2-(3-bromothiophen-2-yl)acetonitrile (1.0 g) and ethyl formate (3.7 g) in dimethyl sulfoxide (5.0 mL) was added sodium ethoxide (20% solution in ethanol, 3.1 mL), and the mixture was stirred at room temperature for 3 hours. 2.5 mol/L hydrochloric acid ethanol solution (3.6 mL) and 4-amino-2-hydroxybenzoic acid (0.9 g) were added to reaction solution. The mixture was stirred at 50° C. for 5 hours. To the reaction solution was added water. The precipitated solid was collected by filtration, washed with water, and dried under reduced pressure at 50° C. for 3 hours. The obtained residue was purified by column chromatography on silica gel (eluent: dichloromethane/methanol=87/13−78/22) to give the condensate (0.91 g). To a solution of this condensate (0.91 g) in dimethyl sulfoxide (4.5 mL) were added copper(I) iodide (47 mg), ethylene glycol (0.3 g) and tripotassium phosphate (1.1 g), and the mixture was stirred at 80° C. for 5 hours. After cooling to 50° C., to the mixture was added 2 mol/L hydrochloric acid (8.7 mL) and the mixture was stirred at room temperature for 1 hour. The precipitated solid was collected by filtration, washed with mixed solution of water and dimethyl sulfoxide, 1 mol/L hydrochloric acid and water, and dried under reduced pressure at 50° C. to give the title compound (0.45 g).

후처리

  1. stirringThe mixture was stirred at 50° C. for 5 hours
  2. filtrationThe precipitated solid was collected by filtration
  3. washwashed with water
  4. customdried under reduced pressure at 50° C. for 3 hours
  5. customThe obtained residue was purified by column chromatography on silica gel (eluent: dichloromethane/methanol=87/13−78/22)
  6. customto give the condensate (0.91 g)
  7. stirringthe mixture was stirred at 80° C. for 5 hours
  8. temperatureAfter cooling to 50° C., to the mixture
  9. stirringthe mixture was stirred at room temperature for 1 hour
  10. filtrationThe precipitated solid was collected by filtration
  11. washwashed with mixed solution of water and dimethyl sulfoxide, 1 mol/L hydrochloric acid and water
  12. customdried under reduced pressure at 50° C.

출처 및 근거

ORD 기록
ord-91feb121955143cc810162568358f0bd
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09115144B2

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