Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | Methyl 3-amino-2-thiophenecarboxylate | HCID 89652 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178518411 | HCID 178518411 | — |
Reaction Steps
A solid mixture of methyl 3-aminothiophene-2-carboxylate (40.0 g, 254 mmol) and urea (99.4 g, 163 mmol) was stirred and heated to 180° C. for 5 h. The now semi-fluid mixture was cooled to 75-80° C. before water (800 ml) was added. After stirring at room temperature for 2 h the formed precipitate was filtered off, washed with further water and dried at 40° C. i. vac. Thieno[3,2-d]pyrimidine-2,4-diol was obtained as cream-coloured powder (37.15 g, 87% yield) of >95% purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354415B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-3a49e30c9dd14abc9a72749b7d4ab43b |
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| Source note | uspto-grants-2013_01 |
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