2-[4-[4-Methoxy-benzyl)-piperidin-1-yl]-2-oxo-N-(2-oxo-2,3-dihydro-benzoxazol-6-yl)-acetamide → 1-Piperidineacetamide,n-(2,3-dihydro-2-oxo-6-benzoxazolyl)-4-[(4-hydroxyphenyl)methyl]-a-oxo-

HRID 2115149Notes

Reaction equation

HRID 2115149 reaction equation
C[O:2][C:3]1[CH:30]=[CH:29][C:6]([CH2:7][CH:8]2[CH2:13][CH2:12][N:11]([C:14](=[O:28])[C:15]([NH:17][C:18]3[CH:27]=[CH:26][C:21]4[NH:22][C:23](=[O:25])[O:24][C:20]=4[CH:19]=3)=[O:16])[CH2:10][CH2:9]2)=[CH:5][CH:4]=1>C(OCC)C>[OH:2][C:3]1[CH:30]=[CH:29][C:6]([CH2:7][CH:8]2[CH2:13][CH2:12][N:11]([C:14](=[O:28])[C:15]([NH:17][C:18]3[CH:27]=[CH:26][C:21]4[NH:22][C:23](=[O:25])[O:24][C:20]=4[CH:19]=3)=[O:16])[CH2:10][CH2:9]2)=[CH:5][CH:4]=1

Participants

3

Procedure

The title compound is prepared from 2-[4-(4-methoxy-benzyl)-piperidin-1-yl]-2-oxo-N-(2-oxo-2,3-dihydro-benzoxazol-6-yl)-acetamide (Example 122) according to the method described in Example 192. Melting Point:235-239° C. (diethylether)

Sources & evidence

ORD record
ord-01c004a5a83f4124b26e87c5269e70a9
Source dataset
uspto-grants-2008_10
Patent number
US07435744B2

Reaction notes

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