Formamide → HCID 178518069, compound
Reaction equation
[NH2:1][C:2]1[S:3][CH:4]=[C:5]([C:12]2[O:13][CH:14]=[CH:15][CH:16]=2)[C:6]=1[C:7](OCC)=[O:8].[CH:17]([NH2:19])=O>>[O:13]1[CH:14]=[CH:15][CH:16]=[C:12]1[C:5]1[C:6]2[C:7]([OH:8])=[N:19][CH:17]=[N:1][C:2]=2[S:3][CH:4]=1Participants
3
Procedure
Ethyl 2-amino-4-(2-furyl)thiophene-3-carboxylate (500 mg, 2.1 mmol) in formamide (4 ml) was stirred at 180° C. for 3 hours. The precipitate obtained by cooling the reaction mixture was filtered to obtain 5-(2-furyl)-4-hydroxythieno[2,3-d]pyrimidine (330 mg, 1.5 mmol) having the following physical properties:
Workup
- customThe precipitate obtained
- temperatureby cooling the reaction mixture
- filtrationwas filtered
Sources & evidence
- ORD record
- ord-43803cbfbb4446edb10e189fe92114dd
- Source dataset
- uspto-grants-2004_03
- Patent number
- US06703421B1
Reaction notes
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