HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-(chloromethyl)-3-methyl-1-(1-methylethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Methyl-1-(1-methylethyl)thieno[2,3-d]pyrimidine-2,4(1h,3h)-dione | HCID 18366630 | — |
| Product | 6-(chloromethyl)-3-methyl-1-(1-methylethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione | HCID 18366626 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Aqueous formaldehyde (37%, 2.5 ml) was added to a stirred solution of 3-methyl-1-(1-methylethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (1.0 g) in concentrated hydrochloric acid (5 ml) at 0° C. The mixture was saturated with hydrogen chloride gas and stirred at 0° C. for 3 hours and then at room temperature for 3 days. Ethyl acetate (100 ml) was added, the mixture was washed with water (100 ml) and then with saturated aqueous sodium bicarbonate solution (100 ml), then dried over anhydrous magnesium sulfate, filtered and evaporated to give the subtitle compound (1.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06300334B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-c7adc1211dd84281b589b36e5e0f4b92 |
| Source note | uspto-grants-2001_10 |