HCID 10393535, compound → HCID 69315713, compound

HRID 1392436Notes

Reaction equation

HRID 1392436 reaction equation
[CH2:1]([N:3]([CH2:40][CH3:41])[C:4]1[CH:39]=[CH:38][C:7]([C:8]([NH:10][C:11]2([C:17]([NH:19][CH:20]3[CH2:25][CH2:24][N:23]([C:26]4[CH:31]=[CH:30][C:29]([F:32])=[CH:28][C:27]=4[S:33]([CH3:36])(=[O:35])=[O:34])[CH2:22][C:21]3=[O:37])=[O:18])[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]2)=[O:9])=[CH:6][CH:5]=1)[CH3:2].[ClH:42].C(OCC)(=O)C>>[ClH:42].[CH2:40]([N:3]([CH2:1][CH3:2])[C:4]1[CH:5]=[CH:6][C:7]([C:8]([NH:10][C:11]2([C:17]([NH:19][CH:20]3[CH2:25][CH2:24][N:23]([C:26]4[CH:31]=[CH:30][C:29]([F:32])=[CH:28][C:27]=4[S:33]([CH3:36])(=[O:34])=[O:35])[CH2:22][C:21]3=[O:37])=[O:18])[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]2)=[O:9])=[CH:38][CH:39]=1)[CH3:41]

Participants

3

Procedure

50 ml of saturated hydrogenchloride-ethyl acetate solution was added to 4-[N-[1-[N-(4-(diethylamino)benzoyl)amino]cyclohexanecarbonyl]amino]-1-(4-fluoro-2-methanesulfonylphenyl)piperidin-3-one (500 mg) obtained in Example 172. The reaction mixture was stirred for 2 hours at room temperature and filtered to give 440 mg of the titled compound as white solid.

Workup

  1. filtrationfiltered

Sources & evidence

ORD record
ord-a5a66a66f4e14891b081804f592d476f
Source dataset
uspto-grants-2008_03
Patent number
US07342027B2

Reaction notes

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