Benzeneacetic acid, 3,5-difluoro-α-hydroxy-, (αS)- → HCID 131723829, compound

HRID 133258Notes

Reaction equation

HRID 133258 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:10]=[C:11]([F:13])[CH:12]=1)[C@H:5]([OH:9])[C:6]([OH:8])=O.Cl.[NH2:15][C@H:16]([C:20]([NH:22][N:23]1[C:29](=[O:30])[CH:28]([CH3:31])[C:27]2[CH:32]=[CH:33][C:34]([F:36])=[CH:35][C:26]=2[C:25]2[CH:37]=[CH:38][CH:39]=[CH:40][C:24]1=2)=[O:21])[CH:17]([CH3:19])[CH3:18]>>[F:13][C:11]1[CH:10]=[C:4]([CH:3]=[C:2]([F:1])[CH:12]=1)[C@H:5]([OH:9])[C:6]([NH:15][C@H:16]([C:20]([NH:22][N:23]1[C:29](=[O:30])[CH:28]([CH3:31])[C:27]2[CH:32]=[CH:33][C:34]([F:36])=[CH:35][C:26]=2[C:25]2[CH:37]=[CH:38][CH:39]=[CH:40][C:24]1=2)=[O:21])[CH:17]([CH3:19])[CH3:18])=[O:8]

Participants

3

Reactant 2

HCID 6951479Benzeneacetic acid, 3,5-difluoro-α-hydroxy-, (αS)-HCID 23552795HCID 23552795, compound

Product 1

HCID 131723829HCID 131723829, compound

Procedure

Following General Procedure D and using (S)-3,5-difluoromandelic acid (Example L) and 5-(L-valinyl)-amino-10-fluoro-7-methyl-5,7-dihydro-6H-dibenz[b,d]azepin-6-one hydrochloride (Example 7-W), the title compound was prepared. The product was purified by chromatography (silica, 2.5% MeOH/CHCl3).

Workup

  1. customThe product was purified by chromatography (silica, 2.5% MeOH/CHCl3)

Sources & evidence

ORD record
ord-32663ef3f3394e40a4ea933df78d58f0
Source dataset
uspto-grants-2008_06
Patent number
US07390801B2

Reaction notes

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