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2,4-Dichloro-N-methylaniline → N-(2,4-dichlorophenyl)-8-fluoro-N-methyl-4H-thieno[3,2-c]chromene-2-carboxamide

HRID 628120
Notes
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Reaction equation

HRID 628120 reaction equation
[F:1][C:2]1[CH:11]=[CH:10][C:9]2[O:8][CH2:7][C:6]3[CH:12]=[C:13]([C:15](Cl)=[O:16])[S:14][C:5]=3[C:4]=2[CH:3]=1.[Cl:18][C:19]1[CH:26]=[C:25]([Cl:27])[CH:24]=[CH:23][C:20]=1[NH:21][CH3:22]>>[Cl:18][C:19]1[CH:26]=[C:25]([Cl:27])[CH:24]=[CH:23][C:20]=1[N:21]([CH3:22])[C:15]([C:13]1[S:14][C:5]2[C:4]3[CH:3]=[C:2]([F:1])[CH:11]=[CH:10][C:9]=3[O:8][CH2:7][C:6]=2[CH:12]=1)=[O:16]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 28009352,4-Dichloro-N-methylanilineHCID 579004718-fluoro-4H-thieno[3,2-c]chromene-2-carbonyl chloride

Product 1

HCID 57900488N-(2,4-dichlorophenyl)-8-fluoro-N-methyl-4H-thieno[3,2-c]chromene-2-carboxamide

Procedure

Following Example 75, 8-fluoro-4H-thieno[3,2-c]chromene-2-carbonyl chloride and 2,4-dichloro-N-methylaniline gave 164bp. MS: (ESI+)=408.0

Workup

  1. customgave 164bp

Sources & evidence

ORD record
ord-831edb5795164a459bd2e432a4b892e4
Source dataset
On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09309265B2

Reaction notes

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