2,4,5-Trichloropyrimidine → HCID 86625360, compound
Reaction equation
[CH3:1][O:2][C:3]([C:5]1[C:13]2[CH:12]=[C:11]([C:14]3[CH:19]=[CH:18][N:17]=[C:16]([Cl:20])[N:15]=3)[S:10][C:9]=2[CH:8]=[CH:7][CH:6]=1)=[O:4].COC(C1C2C=CSC=2C=CC=1)=O.[Cl:34]C1N=C(Cl)C(Cl)=CN=1>>[CH3:1][O:2][C:3]([C:5]1[C:13]2[CH:12]=[C:11]([C:14]3[C:19]([Cl:34])=[CH:18][N:17]=[C:16]([Cl:20])[N:15]=3)[S:10][C:9]=2[CH:8]=[CH:7][CH:6]=1)=[O:4]Participants
4
Procedure
Using the method of 2-(2-chloropyrimidin-4-yl)-benzo[b]thiophene-4-carboxylic acid methyl ester, the title compound is synthesized from benzo[b]thiophene-4-carboxylic acid methyl ester and 2,4,5-trichloropyrimidine and isolated as a solid.
Workup
- customisolated as a solid
Sources & evidence
- ORD record
- ord-d22ede3cebcd448d8ea80f118f454cfb
- Source dataset
- uspto-grants-2009_06
- Patent number
- US07547691B2
Reaction notes
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