Sodium borohydride → HCID 86636460, compound

HRID 1664431Notes

Reaction equation

HRID 1664431 reaction equation
[BH4-].[Na+].[F:3][CH:4]([F:33])[CH2:5][O:6][C:7]1[N:14]=[C:13]([O:15][C:16]2[CH:21]=[CH:20][C:19]([B:22]3[O:26]C(C)(C)C(C)(C)[O:23]3)=[C:18]([CH:31]=O)[CH:17]=2)[CH:12]=[CH:11][C:8]=1[C:9]#[N:10]>CO.C(Cl)Cl>[F:33][CH:4]([F:3])[CH2:5][O:6][C:7]1[N:14]=[C:13]([O:15][C:16]2[CH:21]=[CH:20][C:19]3[B:22]([OH:26])[O:23][CH2:31][C:18]=3[CH:17]=2)[CH:12]=[CH:11][C:8]=1[C:9]#[N:10]

Participants

5

Procedure

A solution of NaBH4 (0.100 g, 2.6 mmol) in anhydrous methanol (20 mL) was added to a solution of 2-(2,2-difluoro-ethoxy)-6-[3-formyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-nicotinonitrile (5.20 g, 12.1 mmol) in CH2Cl2 (80 mL) and stirred at room temperature for 5 minutes. Solid NaBH4 (0.815 g, 21.5 mmol) was then added portionwise over 30 minutes to the reaction at room temperature and the reaction stirred for an additional 30 minutes. The reaction was quenched by the addition of 60% aqueous acetic acid (5 mL), stirred for 30 minutes at room temperature then concentrated in vacuo. The residue was purified by silica gel flash column chromatography (AcOH/MeOH/CH2Cl2 1:1:100 v/v/v) to give the title compound as a viscous oil which was lyophilized to give a white solid (1.92 g, 48% yield).

Workup

  1. stirringthe reaction stirred for an additional 30 minutes
  2. customThe reaction was quenched by the addition of 60% aqueous acetic acid (5 mL)
  3. stirringstirred for 30 minutes at room temperature
  4. concentrationthen concentrated in vacuo
  5. customThe residue was purified by silica gel flash column chromatography (AcOH/MeOH/CH2Cl2 1:1:100 v/v/v)

Sources & evidence

ORD record
ord-148d5439584f4bdfa0bc2125bd54cde7
Source dataset
uspto-grants-2011_10
Patent number
US08039450B2

Reaction notes

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