(Benzyloxy)acetic acid → HCID 57647119, compound

HRID 1714887Notes

Reaction equation

HRID 1714887 reaction equation
[F:1][C:2]([F:24])([F:23])[C:3]1[CH:22]=[CH:21][CH:20]=[CH:19][C:4]=1[O:5][CH:6]1[CH2:11][CH2:10][N:9]([C:12]2[N:17]=[CH:16][C:15]([NH2:18])=[CH:14][CH:13]=2)[CH2:8][CH2:7]1.[CH2:25]([O:32][CH2:33][C:34](O)=[O:35])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>>[CH2:25]([O:32][CH2:33][C:34]([NH:18][C:15]1[CH:16]=[N:17][C:12]([N:9]2[CH2:8][CH2:7][CH:6]([O:5][C:4]3[CH:19]=[CH:20][CH:21]=[CH:22][C:3]=3[C:2]([F:1])([F:23])[F:24])[CH2:11][CH2:10]2)=[CH:13][CH:14]=1)=[O:35])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1

Participants

3

Procedure

The title compound was prepared in the same manner as described for Example 25, step 2 from 6-{4-[2-(trifluoromethyl)phenoxy]piperidin-1-yl}pyridin-3-amine and benzyloxyacetic acid.

Sources & evidence

ORD record
ord-e8fa2656c0ce48c99cb852ea3fc1794b
Source dataset
uspto-grants-2010_09
Patent number
US07799787B2

Reaction notes

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