Sodium hydride → HCID 66707388, compound

HRID 558319Notes

Reaction equation

HRID 558319 reaction equation
[CH2:1]([C:3]1[NH:7][N:6]=[C:5]([CH:8]([OH:10])[CH3:9])[C:4]=1[O:11][C:12]1[CH:13]=[C:14]([C:20]#[N:21])[CH:15]=[C:16]([CH:19]=1)[C:17]#[N:18])[CH3:2].Br[CH2:23][CH2:24][O:25][CH:26]1[CH2:31][CH2:30][CH2:29][CH2:28][O:27]1.[H-].[Na+]>CN(C)C=O>[CH2:1]([C:3]1[N:7]([CH2:23][CH2:24][O:25][CH:26]2[CH2:31][CH2:30][CH2:29][CH2:28][O:27]2)[N:6]=[C:5]([CH:8]([OH:10])[CH3:9])[C:4]=1[O:11][C:12]1[CH:19]=[C:16]([C:17]#[N:18])[CH:15]=[C:14]([CH:13]=1)[C:20]#[N:21])[CH3:2]

Participants

5

Procedure

To a stirred solution of the pyrazole from Example 263 (197 mg, 0.70 mmol) in dimethylformamide (3 ml) at 0° C. was added 2-(2-bromoethoxy)tetrahydro-2H-pyran (105 μl, 0.70 mmol) followed by sodium hydride (31 mg, 0.77 mmol). After 15 minutes the cooling bath was removed and the mixture was stirred at room temperature for 60 hours. The reaction mixture was quenched by addition of saturated aqueous ammonium chloride solution (0.5 ml) and then concentrated under reduced pressure. The crude product mixture was purified by flash chromatography on silica gel eluting with dichloromethane:methanol (a gradient from 100:0 to 95:5, by volume) to provide the title compound (84 mg) as a white foam which reverts to an oil on standing.

Workup

  1. customAfter 15 minutes the cooling bath was removed
  2. customThe reaction mixture was quenched by addition of saturated aqueous ammonium chloride solution (0.5 ml)
  3. concentrationconcentrated under reduced pressure
  4. customThe crude product mixture was purified by flash chromatography on silica gel eluting with dichloromethane

Sources & evidence

ORD record
ord-8f7b391c22a64c0fa0b610884dd02afd
Source dataset
uspto-grants-2011_11
Patent number
US08063044B2

Reaction notes

Loading…