Diisopropyl Ether → HCID 69100987, compound

HRID 2115063Notes

Reaction equation

HRID 2115063 reaction equation
[F:1][C:2]([F:11])([F:10])[C:3]1[CH:9]=[CH:8][C:6]([NH2:7])=[CH:5][CH:4]=1.[F:12][C:13]1[CH:30]=[CH:29][C:16]([CH2:17][CH:18]2[CH2:23][CH2:22][N:21]([C:24](=[O:28])[C:25](O)=[O:26])[CH2:20][CH2:19]2)=[CH:15][CH:14]=1.C(OC(C)C)(C)C>>[F:12][C:13]1[CH:30]=[CH:29][C:16]([CH2:17][CH:18]2[CH2:19][CH2:20][N:21]([C:24](=[O:28])[C:25]([NH:7][C:6]3[CH:8]=[CH:9][C:3]([C:2]([F:10])([F:11])[F:1])=[CH:4][CH:5]=3)=[O:26])[CH2:22][CH2:23]2)=[CH:15][CH:14]=1

Participants

4

Reactant 3

HCID 7914Diisopropyl EtherHCID 99644-(Trifluoromethyl)anilineHCID 51342220[4-(4-Fluorobenzyl)piperidin-1-yl](oxo)acetic acid

Product 1

HCID 69100987HCID 69100987, compound

Procedure

The title compound is prepared from 4-(trifluoromethyl)-aniline and [4-(4-fluoro-benzyl)-piperidin-1-yl]-oxo-acetic-acid (Example 1b) according to the method described in Example 1c. Melting Point: 109-111° C. (diisopropylether)

Sources & evidence

ORD record
ord-1ba357521a124ccd8eec4f2cd264f867
Source dataset
uspto-grants-2008_10
Patent number
US07435744B2

Reaction notes

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