Isopropylamine → HCID 54577589, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:16]([O:17][CH3:18])=[CH:15][CH:14]=[C:13]([C:19]2[CH:20]=[C:21]3[C:25](=[CH:26][CH:27]=2)[C:24](=[O:28])[CH2:23][CH2:22]3)[C:4]=1[O:5][CH2:6][C:7]([CH3:12])([CH3:11])[C:8]([OH:10])=O.[CH:29]([NH2:32])([CH3:31])[CH3:30].COC1C(OC)=CC=C(C2C=C3C(=CC=2)C(=O)CC3)C=1OCC(C)(C)C(NC)=O>>[CH3:1][O:2][C:3]1[C:16]([O:17][CH3:18])=[CH:15][CH:14]=[C:13]([C:19]2[CH:20]=[C:21]3[C:25](=[CH:26][CH:27]=2)[C:24](=[O:28])[CH2:23][CH2:22]3)[C:4]=1[O:5][CH2:6][C:7]([CH3:11])([CH3:12])[C:8]([NH:32][CH:29]([CH3:31])[CH3:30])=[O:10]Participants
4
Procedure
From 3-[2,3-Dimethoxy-6-(1-oxo-indan-5-yl)-phenoxy]-2,2-dimethyl-propionic acid (Compound 205) and isopropylamine following the procedure for preparation of Compound 206. Purification by column chromatography (silica gel, 0-40% ethyl acetate in pet ether) afforded the title compound as a solid.
Workup
- customPurification by column chromatography (silica gel, 0-40% ethyl acetate in pet ether)
Sources & evidence
- ORD record
- ord-919dad7393734b5b844fdfe6d9f2996d
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09051290B2
Reaction notes
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