HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → HCID 12934727, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Indole-2-carboxylic acid | HCID 72899 | — |
| Reactant | HCID 178480417 | HCID 178480417 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12934727 | HCID 12934727 | — |
Reaction Steps
A solution of 28.98 g of indole-2-carboxylic acid in 300 ml of methanol is added to a well-stirred solution of 90 g of potassium iodide and 45.6 g of iodine in 270 ml of water at room temperature. This mixture is further treated with a solution of 23.4 g of 1-methyl-1,4,5,6-tetrahydro-2-pyrimidinethiol in 420 ml of warm methanol. The reaction mixture is stirred for 2 hours at room temperature and worked up in the manner described unter Example 1 to yield 3-(1-methyl-1,4,5,6-tetrahydro-2-pyrimidinylthio)-indole-2-carboxylic acid hydriodide which melts at 230°-231° after recrystallization from a mixture of methanol, ethyl acetate and ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04055647 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-f3906a242a6d450ba14d9a8978e1c707 |
| Source note | uspto-grants-1977_10 |