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3-Benzenesulfonylthiophene-2-carbaldehyde → [3-(3-Benzenesulfonylthiophen-2-ylmethyl)-5-fluoro-2-methylindol-1-yl]acetic acid methyl ester

HRID 1944398
Notes
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Reaction equation

HRID 1944398 reaction equation
[CH3:1][O:2][C:3](=[O:16])[CH2:4][N:5]1[C:13]2[C:8](=[CH:9][C:10]([F:14])=[CH:11][CH:12]=2)[CH:7]=[C:6]1[CH3:15].[C:17]1([S:23]([C:26]2[CH:30]=[CH:29][S:28][C:27]=2[CH:31]=O)(=[O:25])=[O:24])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[CH3:1][O:2][C:3](=[O:16])[CH2:4][N:5]1[C:13]2[C:8](=[CH:9][C:10]([F:14])=[CH:11][CH:12]=2)[C:7]([CH2:31][C:27]2[S:28][CH:29]=[CH:30][C:26]=2[S:23]([C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)(=[O:25])=[O:24])=[C:6]1[CH3:15]
ParticipantsProcedureSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 9162623-Benzenesulfonylthiophene-2-carbaldehydeHCID 58247161Methyl 2-(5-fluoro-2-methyl-1H-indol-1-yl)acetate

Product 1

HCID 67043955[3-(3-Benzenesulfonylthiophen-2-ylmethyl)-5-fluoro-2-methylindol-1-yl]acetic acid methyl ester

Procedure

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

Sources & evidence

ORD record
ord-6daa581c9c564e8ab446256a83d15f54
Source dataset
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08394836B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes