HCID 67954034, compound → HCID 67953928, compound

HRID 2178574Notes

Reaction equation

HRID 2178574 reaction equation
C(OC([N:8]([C:22]1[N:23]=[C:24]2[CH:29]=[CH:28][C:27]([Cl:30])=[CH:26][N:25]2[C:31]=1[CH3:32])[S:9]([C:12]1[CH:21]=[CH:20][C:15]([C:16]([O:18][CH3:19])=[O:17])=[CH:14][CH:13]=1)(=[O:11])=[O:10])=O)(C)(C)C>Cl.O1CCOCC1>[ClH:30].[Cl:30][C:27]1[CH:28]=[CH:29][C:24]2[N:25]([C:31]([CH3:32])=[C:22]([NH:8][S:9]([C:12]3[CH:21]=[CH:20][C:15]([C:16]([O:18][CH3:19])=[O:17])=[CH:14][CH:13]=3)(=[O:11])=[O:10])[N:23]=2)[CH:26]=1

Participants

4

Procedure

Compound 15-C (0.820 g, 1.71 mmol) was dissolved in 4N HCl in dioxane (44 mL) and the reaction mixture was stirred for 24 h at room temperature. The solvent was evaporated in vacuo and the crude product was washed with ethyl ether. The resulting solid was filtered, washed with additional ethyl ether, and dried in vacuo to give compound 15-D as a white solid (0.610 g, 86%); MS m/z (M+H+) 380.

Workup

  1. customThe solvent was evaporated in vacuo
  2. washthe crude product was washed with ethyl ether
  3. filtrationThe resulting solid was filtered
  4. washwashed with additional ethyl ether
  5. customdried in vacuo
  6. customto give compound 15-D as a white solid (0.610 g, 86%)

Sources & evidence

ORD record
ord-cf32a8e2107146f89ac79e772ba10bfd
Source dataset
uspto-grants-2015_06
Patent number
US09067935B2

Reaction notes

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