Sodium borohydride → HCID 23114129, compound

HRID 1787336Notes

Reaction equation

HRID 1787336 reaction equation
[C:1]([C:4]1[C:12]2[O:11][CH2:10][CH:9]([C:13]3[CH:18]=[CH:17][C:16]([CH:19]([CH3:21])[CH3:20])=[CH:15][CH:14]=3)[C:8]=2[C:7]([CH3:22])=[C:6]([NH:23][C:24]([NH:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[O:25])[C:5]=1[CH3:31])(=[O:3])[CH3:2].[BH4-].[Na+]>CO.O>[C:27]([NH:26][C:24]([NH:23][C:6]1[C:5]([CH3:31])=[C:4]([CH:1]([OH:3])[CH3:2])[C:12]2[O:11][CH2:10][CH:9]([C:13]3[CH:14]=[CH:15][C:16]([CH:19]([CH3:21])[CH3:20])=[CH:17][CH:18]=3)[C:8]=2[C:7]=1[CH3:22])=[O:25])([CH3:29])([CH3:28])[CH3:30]

Participants

5

Procedure

To a solution of N-(7-acetyl-3-(4-isopropylphenyl)-4,6-dimethyl-2,3-dihydro-1-benzofuran-5-yl)-N′-(tert-butyl)urea (718 mg, 1.7 mmol) obtained in Example 204 in methanol (10 mL) was added sodium borohydride (64.3 mg, 1.7 mmol) at 0° C., and the resulting mixture was stirred for 3 hours. The reaction solution was diluted with water and the product was extracted with ethyl acetate. The extract was washed with saturated brine, dried over sodium sulfate, and then concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to obtain 115 mg (yield: 16%) of the title compound having high polarity of two isomers. Melting point: 212-214° C. (ethyl acetate-hexane).

Workup

  1. extractionthe product was extracted with ethyl acetate
  2. washThe extract was washed with saturated brine
  3. dry with materialdried over sodium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1)

Sources & evidence

ORD record
ord-d07e7d4a88b14e7ebe3265d9df62d5b4
Source dataset
uspto-grants-2009_03
Patent number
US07507841B2

Reaction notes

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