HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → HCID 12934723, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 5-Methoxyindole-2-carboxylic acid | HCID 20401 | — |
| Reactant | HCID 178527864 | HCID 178527864 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12934723 | HCID 12934723 | — |
Reaction Steps
A solution of 5.7 g of 5-methoxy-indole-2-carboxylic acid in 70 ml of hot methanol is added portionwise to a solution of 15 g potassium iodide and 7.6 g of iodine in 45 ml of water. This is further treated with a solution of 3.48 g of 1,4,5,6-tetrahydro-2-pyrimidinethiol in 70 ml of hot methanol, stirred at room temperature for 2 hours and filtered. The filtrate is worked up in the manner described under Example 1 to yield 5-methoxy-3-(1,4,5,6-tetrahydro-2-pyrimidinylthio)-indole-2-carboxylic acid hydriodide which melts at 239°-240° after recrystallization from a mixture of methanol, ethyl acetate and ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03954757 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-eb98674270f143419259b7d20d28b39d |
| Source note | uspto-grants-1976_05 |