Methanol → HCID 178520863, compound

HRID 2233784Notes

Reaction equation

HRID 2233784 reaction equation
CO.[NH:3]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[NH:5][C:4]1=[C:12]([C:28]([C:30]1[CH:35]=[CH:34][CH:33]=[C:32]([F:36])[CH:31]=1)=[O:29])[C:13]([C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([C@@H:21]2[CH2:25][O:24]C(C)(C)[O:22]2)[CH:16]=1)=[O:14].O.C1(C)C=CC(S(O)(=O)=O)=CC=1.C(=O)(O)[O-].[Na+]>O>[NH:3]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[NH:5][C:4]1=[C:12]([C:28]([C:30]1[CH:35]=[CH:34][CH:33]=[C:32]([F:36])[CH:31]=1)=[O:29])[C:13]([C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([C@@H:21]([OH:22])[CH2:25][OH:24])[CH:16]=1)=[O:14]

Participants

6

Procedure

A 20 ml portion of methanol solution containing 1.68 g of 2-(1,3-dihydro-2H-benzimidazol-2-ylidene)-1-{3-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]phenyl}-3-(3-fluorophenyl)propane-1,3-dione was mixed with 560 mg of p-toluenesulfonic acid monohydrate and stirred at room temperature for 18 hours. This was mixed with appropriate amounts of purified water and saturated sodium bicarbonate aqueous solution, extracted with ethyl acetate and dried with anhydrous magnesium sulfate. After concentration, the thus formed residue was purified by a silica gel column chromatography to obtain 640 mg (42%) of 2-(1,3-dihydro-2H-benzimidazol-2-ylidene)-1-{3-[(1R)-1,2-dihydroxyethyl]phenyl}-3-(3-fluorophenyl)propane-1,3-dione (Example 4-1) from a hexane-ethyl acetate (3:1-1:3) eluate.

Workup

  1. extractionextracted with ethyl acetate
  2. dry with materialdried with anhydrous magnesium sulfate
  3. concentrationAfter concentration
  4. customthe thus formed residue was purified by a silica gel column chromatography

Sources & evidence

ORD record
ord-5df38f0d17dd479799918962d64fee17
Source dataset
uspto-grants-2010_05
Patent number
US07709519B2

Reaction notes

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