Sodium borohydride → HCID 67440957, compound

HRID 1483725Notes

Reaction equation

HRID 1483725 reaction equation
[BH4-].[Na+].[CH2:3]([O:5][C:6]1[C:11]([C:12]#[N:13])=[CH:10][N:9]=[C:8]([O:14][C:15]2[CH:20]=[CH:19][C:18]([B:21]3[O:25]C(C)(C)[C:23](C)(C)[O:22]3)=[C:17](C=O)[CH:16]=2)[CH:7]=1)[CH3:4]>CO.C(Cl)Cl>[CH2:3]([O:5][C:6]1[C:11]([C:12]#[N:13])=[CH:10][N:9]=[C:8]([O:14][C:15]2[CH:16]=[CH:17][C:18]3[B:21]([OH:25])[O:22][CH2:23][C:19]=3[CH:20]=2)[CH:7]=1)[CH3:4]

Participants

5

Procedure

A solution of NaBH4 (0.10 g, 2.6 mmol) in anhydrous methanol (20 mL) was added to a solution of 4-ethoxy-6-[3-formyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-nicotinonitrile (3.53 g, 8.95 mmol) in CH2Cl2 (80 mL) and stirred at room temperature for 5 minutes. Solid NaBH4 (0.58 g, 15.3 mmol) was then added portionwise over 30 minutes at room temperature. The reaction mixture was stirred for an additional 30 minutes, quenched by the addition 70% aqueous acetic acid (3 mL) then stirred for an additional 1 hour at room temperature. The reaction was concentrated and the residue 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. The oil was lyophilized to give a white solid (0.781 g, 29% yield).

Workup

  1. stirringThe reaction mixture was stirred for an additional 30 minutes
  2. customquenched by the addition 70% aqueous acetic acid (3 mL)
  3. stirringthen stirred for an additional 1 hour at room temperature
  4. concentrationThe reaction was concentrated
  5. customthe residue purified by silica gel flash column chromatography (AcOH/MeOH/CH2Cl2 1:1:100 v/v/v)

Sources & evidence

ORD record
ord-44c7697d0c15444daab29faf4f2a0b98
Source dataset
uspto-grants-2016_08
Patent number
US09416146B2

Reaction notes

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