Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 20094178 | HCID 20094178 | — |
| Solvent | Ethylorthoformate | HCID 53630039 | — |
| Product | HCID 20093979 | HCID 20093979 | — |
Reaction Steps
4. 15.7 g of 2-(chloromethyl)-4-hydrazinothieno[3,2-d]pyrimidine are suspended in 280ml of ethyl orthoformate. The suspension is heated (bath temp. 125° C.) while stirring and the ethanol which results is distilled off. After 3 h., the mixture is cooled to 0° C., the precipitate is filtered off and washed with ethanol. The product is dried in a vacuum. There are obtained 15.2 g of 5-(chloromethyl)thieno[2,3-e][1,2,4]triazolo[4,3-c]-pyrimidine. m.p. above 400° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05387585 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-9fad027ca04f4e48a3bdb6c8122eedd6 |
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| Source note | uspto-grants-1995_02 |
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