Sodium hydride → HCID 86686961, compound

HRID 2284933Notes

Reaction equation

HRID 2284933 reaction equation
[NH2:1][C@@H:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C@H:5]([OH:12])[CH2:4][CH2:3]1.[H-].[Na+].[C:15]([C:17]1[CH:22]=[CH:21][C:20](F)=[CH:19][N:18]=1)#[N:16]>CN(C=O)C>[NH2:1][C@@H:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C@H:5]([O:12][C:20]2[CH:21]=[CH:22][C:17]([C:15]#[N:16])=[N:18][CH:19]=2)[CH2:4][CH2:3]1

Participants

5

Procedure

Intermediate A (300 mg, 1.84 mmol) was added to an ice cold stirred suspension of sodium hydride (60% in mineral oil, 221 mg, 5.52 mmol) in DMF (15 mL) and stirred for 15 min. 2-Cyano-5-fluoropyridine (224 mg, 1.84 mmol) was added and the reaction warmed to RT. After 90 min, the reaction was quenched by dropwise addition of water and the mixture partitioned between EtOAc (75 mL) and water (150 mL). The aqueous layer was then extracted with EtOAc (3×). The combined organic layers were washed with brine, dried (MgSO4), filtered and evaporated in vacuo. The residue was purified by FCC, using 0-5% [2M NH3 in MeOH] in DCM, to give the title compound (255 mg, 0.96 mmol, 52%). LCMS (Method 4): Rt 0.28, 1.73, m/z 266.1 [MH+].

Workup

  1. stirringstirred for 15 min
  2. customthe reaction was quenched by dropwise addition of water
  3. customthe mixture partitioned between EtOAc (75 mL) and water (150 mL)
  4. extractionThe aqueous layer was then extracted with EtOAc (3×)
  5. washThe combined organic layers were washed with brine
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customevaporated in vacuo
  9. customThe residue was purified by FCC

Sources & evidence

ORD record
ord-21b04a4aa8dd401888dc4a1892a069c5
Source dataset
uspto-grants-2015_09
Patent number
US09145413B2

Reaction notes

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