Potassium bis(trimethylsilyl)amide → HCID 135816395, compound

HRID 1068671Notes

Reaction equation

HRID 1068671 reaction equation
C[Si]([N-][Si](C)(C)C)(C)C.[K+].[CH2:11]([O:13][C:14]1[C:19]([C:20]2[NH:21][C:22](=[O:39])[C:23]3[C:24](=[C:26]([CH2:36][CH2:37][CH3:38])[N:27]([CH2:29][C:30]4[CH:35]=[CH:34][CH:33]=[CH:32][N:31]=4)[N:28]=3)[N:25]=2)=[CH:18][C:17]([S:40]([N:43]2[CH2:48][CH2:47][N:46]([CH2:49][CH3:50])[CH2:45][CH2:44]2)(=[O:42])=[O:41])=[CH:16][N:15]=1)[CH3:12]>OCC1C=COC=1>[CH2:49]([N:46]1[CH2:47][CH2:48][N:43]([S:40]([C:17]2[CH:18]=[C:19]([C:20]3[NH:21][C:22](=[O:39])[C:23]4[C:24](=[C:26]([CH2:36][CH2:37][CH3:38])[N:27]([CH2:29][C:30]5[CH:35]=[CH:34][CH:33]=[CH:32][N:31]=5)[N:28]=4)[N:25]=3)[C:14]([O:13][CH2:11][C:12]3[CH:12]=[CH:11][O:13][CH:14]=3)=[N:15][CH:16]=2)(=[O:41])=[O:42])[CH2:44][CH2:45]1)[CH3:50]

Participants

4

Procedure

Potassium bis(trimethylsilyl)amide (176 mg, 0.88 mmol) was added to a stirred suspension of the title compound of Example 26 (100 mg, 0.17 mmol) in 3-hydroxymethylfuran (4 ml) and the reaction mixture heated under reflux for 24 hours then allowed to cool. The resulting mixture was evaporated under reduced pressure and the residue purified by column chromatography on silica gel, using dichloromethane: methanol (95:5) as eluant, to furnish the title compound (33 mg, 31%) as a pale yellow foam. δ (CDCl3): 0.93 (3H,t), 1.04 (3H,t), 1.72 (2H,m), 2.41 (2H,q), 2.55 (4H,m), 2.99 (2H,t), 3.14 (4H,m), 5.63 (2H,s), 5.68 (2H,s), 6.60 (1H,s), 7.09 (1H,d), 7.22 (1H,m), 7.44 (1H,s), 7.64 (2H,m), 8.57 (1H,d), 8.68 (1H,s), 9.02 (1H,s), 10.53 (1H,s). LRMS: m/z 619 (M+1)+.

Workup

  1. temperaturethe reaction mixture heated
  2. temperatureunder reflux for 24 hours
  3. temperatureto cool
  4. customThe resulting mixture was evaporated under reduced pressure
  5. customthe residue purified by column chromatography on silica gel

Sources & evidence

ORD record
ord-876f8f23deb14d7d882d6ed3056c4de7
Source dataset
uspto-grants-2001_06
Patent number
US06251904B1

Reaction notes

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