HCID 13413612, compound → HCID 67044291, compound

HRID 1944423Notes

Reaction equation

HRID 1944423 reaction equation
[C:1]1([S:7]([C:10]2[S:11][CH:12]=[CH:13][C:14]=2[CH:15]=O)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:17][O:18][C:19](=[O:32])[CH2:20][N:21]1[C:29]2[C:24](=[CH:25][C:26]([F:30])=[CH:27][CH:28]=2)[CH:23]=[C:22]1[CH3:31]>>[CH3:17][O:18][C:19](=[O:32])[CH2:20][N:21]1[C:29]2[C:24](=[CH:25][C:26]([F:30])=[CH:27][CH:28]=2)[C:23]([CH2:15][C:14]2[CH:13]=[CH:12][S:11][C:10]=2[S:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)(=[O:8])=[O:9])=[C:22]1[CH3:31]

Participants

3

Reactant 2

HCID 13413612HCID 13413612, compoundHCID 58247161Methyl 2-(5-fluoro-2-methyl-1H-indol-1-yl)acetate

Product 1

HCID 67044291HCID 67044291, compound

Procedure

The title compound was prepared by the method of Preparation 1c using 2-phenylsulfonylthiophene-3-carbaldehyde and (5-fluoro-2-methylindol-1-yl)acetic acid methyl ester.

Sources & evidence

ORD record
ord-46207d00eb2744ee96b93d09099573f5
Source dataset
uspto-grants-2013_03
Patent number
US08394836B2

Reaction notes

Loading…