Water → HCID 136023069, compound

HRID 1458933Notes

Reaction equation

HRID 1458933 reaction equation
C([O:4][C:5]1[CH:6]=[C:7]([C:15]2[C:24]3[C:19](=[CH:20][C:21]([O:29][CH3:30])=[C:22]([O:25]C(C)C)[CH:23]=3)[N:18]=[C:17]([CH2:31][N:32]3[CH:36]=[N:35][CH:34]=[N:33]3)[C:16]=2[C:37]([O:39][CH2:40][CH3:41])=[O:38])[CH:8]=[CH:9][C:10]=1[O:11]C(C)C)(C)C.O>ClCCl.[Ti](Cl)(Cl)(Cl)Cl>[OH:4][C:5]1[CH:6]=[C:7]([C:15]2[C:24]3[C:19](=[CH:20][C:21]([O:29][CH3:30])=[C:22]([OH:25])[CH:23]=3)[N:18]=[C:17]([CH2:31][N:32]3[CH:36]=[N:35][CH:34]=[N:33]3)[C:16]=2[C:37]([O:39][CH2:40][CH3:41])=[O:38])[CH:8]=[CH:9][C:10]=1[OH:11]

Participants

5

Procedure

Titanium tetrachloride (TiCl4)(316 mg) was added at 0° C. to a solution of ethyl 4-(3,4-diisopropoxyphenyl)-6-isopropoxy-7-methoxy-2-(1,2,4-triazol-1-ylmethyl)quinoline-3-carboxylate (96.0 mg) in dichloromethane (1.0 ml), and the mixture was stirred at the same temperature for 10 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The ethyl acetate layer was washed with a saturated aqueous sodium bicarbonate solution and water, and dried over magnesium sulfate. The solvent was evaporated. The residual oil was subjected to column chromatography on silica gel. The fractions eluted with ethyl acetate/methanol (10/1, v/v) gave ethyl 4-(3,4-dihydroxyphenyl)-6-hydroxy-7-methoxy-2-(1,2,4-triazol-1-ylmethyl)quinoline-3-carboxylate (19.0 mg, 26%). mp. 264°-266° C.

Workup

  1. extractionextracted with ethyl acetate
  2. washThe ethyl acetate layer was washed with a saturated aqueous sodium bicarbonate solution and water
  3. dry with materialdried over magnesium sulfate
  4. customThe solvent was evaporated
  5. washThe fractions eluted with ethyl acetate/methanol (10/1

Sources & evidence

ORD record
ord-b59d1e477543438cb509dfc462ecc17d
Source dataset
uspto-grants-1998_12
Patent number
US05852039

Reaction notes

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