3-Aminobiphenyl → HCID 57541840, compound

HRID 2422309Notes

Reaction equation

HRID 2422309 reaction equation
Br[C:2]1[CH:3]=[C:4]([CH:19]=[CH:20][CH:21]=1)[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][CH2:14][C:15]([O:17]C)=[O:16])=[CH:9][CH:8]=1.[C:22]1([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[CH:27]=[CH:26][CH:25]=[C:24]([NH2:28])[CH:23]=1>>[C:22]1([C:29]2[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=2)[CH:27]=[CH:26][CH:25]=[C:24]([NH:28][C:2]2[CH:3]=[C:4]([CH:19]=[CH:20][CH:21]=2)[CH2:5][O:6][C:7]2[CH:12]=[CH:11][C:10]([CH2:13][CH2:14][C:15]([OH:17])=[O:16])=[CH:9][CH:8]=2)[CH:23]=1

Participants

3

Reactant 2

HCID 167173-AminobiphenylHCID 23136270Methyl 4-[(3-bromophenyl)methoxy]benzenepropanoate

Product 1

HCID 57541840HCID 57541840, compound

Procedure

The title compound was synthesized in the same manner as in Example 298 from methyl 3-[4-[(3-bromobenzyl)oxy]phenyl]propanoate and biphenyl-3-ylamine. colorless crystals (yield 6%).

Sources & evidence

ORD record
ord-8de139220920455da5cfbd5119f4fe9a
Source dataset
uspto-grants-2011_06
Patent number
US07960369B2

Reaction notes

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