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Phosphorus oxychloride → 4-Chloro-2-(pyrazin-2-yl)-6-trifluoromethyl-thieno-[2,3-d]-pyrimidine

HRID 367785
Notes
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Reaction equation

HRID 367785 reaction equation
[C:1]([C:3]1[CH:8]=[N:7][CH:6]=[CH:5][N:4]=1)#[N:2].[NH2:9][C:10]1[S:11][C:12]([C:20]([F:23])([F:22])[F:21])=[CH:13][C:14]=1[C:15](OCC)=O.O=P(Cl)(Cl)[Cl:26]>>[Cl:26][C:15]1[C:14]2[CH:13]=[C:12]([C:20]([F:21])([F:22])[F:23])[S:11][C:10]=2[N:9]=[C:1]([C:3]2[CH:8]=[N:7][CH:6]=[CH:5][N:4]=2)[N:2]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 24813Phosphorus oxychlorideHCID 73172PyrazinecarbonitrileHCID 18460227Ethyl 2-amino-5-(trifluoromethyl)thiophene-3-carboxylate

Product 1

HCID 184600644-Chloro-2-(pyrazin-2-yl)-6-trifluoromethyl-thieno-[2,3-d]-pyrimidine

Procedure

With the procedure of Example 477, the reaction of 2-cyanopyrazine and 2-amino-5-trifluoromethyl-3-ethoxycarbonyl-thiophene, and the subsequent reaction with POCl3 yields 4-chloro-2-(pyrazin-2-yl)-6-trifluoromethyl-thieno-[2,3-d]-pyrimidine

Sources & evidence

ORD record
ord-85a979fab9fa4efabf64abe2dd036d82
Source dataset
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06133271

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes