Hydrochloric Acid → HCID 12150310, compound

HRID 1296843Notes

Reaction equation

HRID 1296843 reaction equation
C=C[C@@H]1[C@@H:8]2[CH2:9][C@H:10]([C@@H:11]([OH:22])[C:12]3[CH:13]=[CH:14]N=C4C=C[CH:19]=[CH:18][C:17]=34)[N:5]([CH2:6][CH2:7]2)C1.N1C=CC=C[CH:24]=1.ClC1C=C[C:33]([C:34]([C:36]2C=CC=CN=2)=[O:35])=CC=1.[ClH:44].[O:45]1CC[CH2:47][CH2:46]1>>[OH:22][C:11]([C:12]1[CH:17]=[CH:18][C:19]([Cl:44])=[CH:14][CH:13]=1)([C:10]1[CH:9]=[CH:8][CH:7]=[CH:6][N:5]=1)[CH2:47][C:46]([O:35][C:34]([CH3:33])([CH3:36])[CH3:24])=[O:45]

Participants

6

Reactant 5

HCID 313Hydrochloric AcidHCID 1049PyridineHCID 8028Tetrahydrofuran2×HCID 80594(4-Chlorophenyl) 2-pyridyl ketoneHCID 90454Cinchonine

Product 1

HCID 12150310HCID 12150310, compoundYield 81%

Procedure

Under argon atmosphere, cinchonine (440 mg, 1.0 mmol) was suspended in tetrahydrofuran (absolute, 2.0 mL), and to this suspension was added a Reformatsky reagent (0.5 M; 8.0 mL, 4.0 mmol) dropwise under ice-cooling. After stirring for 10 minutes, pyridine (0.30 mL, 2 mmol) was added thereto dropwise. After stirring for 20 minutes under ice-cooling, the mixture was cooled to −400° C. A solution of 2-(4-chlorobenzoyl)pyridine (218mg, 1.0 mmol) in tetrahydrofuran (absolute, 4.0 mL) was added dropwise over 10 minutes, and the mixture was stirred at −40° C. for 4 hours. To this reaction solution was added 1N HCl (20 mL), which was then extracted with ethyl acetate (20 mL×2). The extracted solution was washed successively with an aqueous saturated sodium bicarbonate solution and an aqueous saturated sodium chloride solution. After the organic layer was dried with sodium sulfate, the solvent was removed under reduced pressure. The residue was analyzed with high performance liquid chromatography. Consequently, the yield was 81% and the enantiomer excess was 91%.

Workup

  1. additionto this suspension was added a Reformatsky reagent (0.5 M; 8.0 mL, 4.0 mmol) dropwise under ice-
  2. temperaturecooling
  3. stirringAfter stirring for 20 minutes under ice-
  4. temperaturecooling
  5. temperaturethe mixture was cooled to −400° C
  6. stirringthe mixture was stirred at −40° C. for 4 hours
  7. extractionwas then extracted with ethyl acetate (20 mL×2)
  8. washThe extracted solution was washed successively with an aqueous saturated sodium bicarbonate solution
  9. dry with materialAfter the organic layer was dried with sodium sulfate
  10. customthe solvent was removed under reduced pressure

Sources & evidence

ORD record
ord-81b73f2684994af5b0ce79ee7241efb1
Source dataset
uspto-grants-2007_07
Patent number
US07247732B2

Reaction notes

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