Ammonium Chloride → HCID 15908562, compound

HRID 428012Notes

Reaction equation

HRID 428012 reaction equation
[CH3:1][O:2][C:3]1[CH:18]=[CH:17][C:6]([C:7]([NH:9][C:10]2[C:15]([NH2:16])=[CH:14][CH:13]=[CH:12][N:11]=2)=[O:8])=[CH:5][CH:4]=1.C[Si](C)(C)[N-][Si](C)(C)C.[K+].[C:29]([C:33]1[CH:41]=[CH:40][C:36]([C:37](Cl)=[O:38])=[CH:35][CH:34]=1)([CH3:32])([CH3:31])[CH3:30].[Cl-].[NH4+]>O1CCCC1.C(OCC)(=O)C>[C:29]([C:33]1[CH:34]=[CH:35][C:36]([C:37]([NH:16][C:15]2[C:10]([NH:9][C:7](=[O:8])[C:6]3[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:18][CH:17]=3)=[N:11][CH:12]=[CH:13][CH:14]=2)=[O:38])=[CH:40][CH:41]=1)([CH3:32])([CH3:30])[CH3:31]

Participants

7

Procedure

A solution of N2-(4-methoxybenzoyl)-2,3-pyridinediamine (92 mg, 0.38 mmol) in tetrahydrofuran (1 mL) was treated with potassium hexamethyldisilazide (160 mg, 0.80 mmol). After 0.25 hr, the mixture was treated with 4-tert-butylbenzoyl chloride. After 0.75 hr, the mixture was poured into a mixture of aqueous ammonium chloride solution and ethyl acetate. The organic layer was washed twice with water, once with saturated sodium chloride solution, dried (magnesium sulfate), and filtered. Concentration in vacuo and purification of the residue by flash cromatography (silica gel, methylene chloride/ethyl acetate) followed by recrystallization from ethyl acetate/hexanes yielded 31 mg (20%) of the title compound.

Workup

  1. waitAfter 0.75 hr
  2. washThe organic layer was washed twice with water, once with saturated sodium chloride solution
  3. dry with materialdried (magnesium sulfate)
  4. filtrationfiltered
  5. concentrationConcentration
  6. customin vacuo and purification of the residue by flash cromatography (silica gel, methylene chloride/ethyl acetate)
  7. customfollowed by recrystallization from ethyl acetate/hexanes

Sources & evidence

ORD record
ord-24bd7364b39c4af1b09c4093f8d6cde0
Source dataset
uspto-grants-2001_11
Patent number
US06313151B1

Reaction notes

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