4,7-Difluoro-2-[3-methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid → 4,7-Difluoro-2-(2-isobutyl-3-methyl-benzoylamino)-indan-2-carboxylic acid
Reaction equation
[F:1][C:2]1[CH:10]=[CH:9][C:8]([F:11])=[C:7]2[C:3]=1[CH2:4][C:5]([NH:15][C:16](=[O:28])[C:17]1[CH:22]=[CH:21][CH:20]=[C:19]([CH3:23])[C:18]=1[CH:24]=[C:25]([CH3:27])[CH3:26])([C:12]([OH:14])=[O:13])[CH2:6]2>CO.[Pd]>[F:1][C:2]1[CH:10]=[CH:9][C:8]([F:11])=[C:7]2[C:3]=1[CH2:4][C:5]([NH:15][C:16](=[O:28])[C:17]1[CH:22]=[CH:21][CH:20]=[C:19]([CH3:23])[C:18]=1[CH2:24][CH:25]([CH3:26])[CH3:27])([C:12]([OH:14])=[O:13])[CH2:6]2Participants
4
Procedure
A solution of 4,7-difluoro-2-[3-methyl-2-(2-methyl-propenyl)-benzoylamino]-indan-2-carboxylic acid (392) (82 mg, 0.21 mmol) in MeOH (40 mL) is hydrogenated using 10% palladium/carbon catalyst at 40 bar and 30° C. using the Thales nanotechnology H-Cube for 5 h. The MeOH is concentrated to dryness in vacuo to give the product (393) as white solid powder.
Workup
- customat 40 bar and 30° C.
- customfor 5 h
- concentrationThe MeOH is concentrated to dryness in vacuo
Sources & evidence
- ORD record
- ord-5f25f27644b84088bf321672800b0faa
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08569535B2
Reaction notes
Loading…