4-Piperidinecarbonitrile, 4-phenyl- → HCID 58928304, compound

HRID 852173Notes

Reaction equation

HRID 852173 reaction equation
[F:1][C:2]1[CH:21]=[CH:20][C:5]2[C:6]([C:9]3[CH:14]=[CH:13][C:12]([O:15][CH2:16][C@H:17]4[CH2:19][O:18]4)=[CH:11][CH:10]=3)=[N:7][O:8][C:4]=2[CH:3]=1.[C:22]([C:24]1([C:30]2[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=2)[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]1)#[N:23]>CN(C)C=O.C(O)C>[F:1][C:2]1[CH:21]=[CH:20][C:5]2[C:6]([C:9]3[CH:10]=[CH:11][C:12]([O:15][CH2:16][C@H:17]([OH:18])[CH2:19][N:27]4[CH2:26][CH2:25][C:24]([C:30]5[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=5)([C:22]#[N:23])[CH2:29][CH2:28]4)=[CH:13][CH:14]=3)=[N:7][O:8][C:4]=2[CH:3]=1

Participants

5

Procedure

The title compound is prepared from a mixture of (R)-6-fluoro-3-(4-oxiranylmethoxy-phenyl)-benzo[d]isoxazole in dimethylformamide and 4-cyano-4-phenylpiperidine in ethanol, essentially as described above in Example 70. Purity by LC/MS=<100%, [M+H]+=472.

Sources & evidence

ORD record
ord-6556ba92614749029a0ed7254a0b864b
Source dataset
uspto-grants-2007_08
Patent number
US07253165B2

Reaction notes

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