Sodium hydride → HCID 10869178, compound

HRID 1988579Notes

Reaction equation

HRID 1988579 reaction equation
[H-].[Na+].[C:3]([O:7][C:8]([NH:10][C:11]1[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][CH:12]=1)=[O:9])([CH3:6])([CH3:5])[CH3:4].[N+](C1C=C(S(O[CH2:31][C@H:32]2[O:34][CH2:33]2)(=O)=O)C=CC=1)([O-])=O>CN(C)C=O>[C:3]([O:7][C:8]([NH:10][C:11]1[CH:12]=[CH:13][C:14]([O:17][CH2:31][C@H:32]2[O:34][CH2:33]2)=[CH:15][CH:16]=1)=[O:9])([CH3:6])([CH3:4])[CH3:5]

Participants

5

Reactant 3

HCID 24758Sodium hydrideHCID 146490Benzenesulfonic acid, 3-nitro-, (2S)-2-oxiranylmethyl esterHCID 2756771N-Boc-4-hydroxyaniline

Product 1

HCID 10869178HCID 10869178, compoundYield 83%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

To an 8 ml dimethylformamide suspension of 60 mg of sodium hydride was added, under ice cooling, 300 mg of 4-(tert-butoxycarbonylamino)phenol. The resultant mixture was stirred at room temperature for 1 hour. Under ice cooling, 372 mg of (S)-glycidyl 3-nitrobenzenesulfonate was gradually added, then the resultant mixture was stirred at room temperature for 2 hours. The reaction was quenched with a 5 ml of saturated aqueous ammonium chloride solution, then the product was extracted with ether. The extract was washed with saturated saline, dried, filtered, then concentrated under reduced pressure to give a residue, which was then purified by silica gel column.chromatography (hexane:ethyl acetate=3:1) to give the above-referenced compound (9) in an amount of 315 mg (yield 83%).

Workup

  1. additionwas added, under ice cooling
  2. customThe reaction was quenched with a 5 ml of saturated aqueous ammonium chloride solution
  3. extractionthe product was extracted with ether
  4. washThe extract was washed with saturated saline
  5. customdried
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customto give a residue, which
  9. customwas then purified by silica gel column.chromatography (hexane:ethyl acetate=3:1)

Sources & evidence

ORD record
ord-7c70571bb1e64a3ab093931ce3e110f5
Source dataset
uspto-grants-2010_01
Patent number
US07642262B2

Reaction notes

Loading…