HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → Ethyl 6-iodo-4-(methoxymethyl)-9H-pyrido[3,4-b]indole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | HCID 13041786 | HCID 13041786 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 6-iodo-4-(methoxymethyl)-9H-pyrido[3,4-b]indole-3-carboxylate | HCID 13041796 | — |
Reaction Steps
A solution of 1.0 g of 4-methoxymethyl-beta-carboline-3-carboxylic-acid-ethylester in 20 ml of methylene chloride and 1.5 ml of pyridine is mixed dropwise with 1.5 ml of iodine chloride at room temperature. After 60 minutes, another 1.5 ml of iodine chloride is added and then 200 mg of iodine. The mixture is stirred for another 2 h at room temperature and then poured into an ice-cold saturated sodium thiosulfate solution, followed by extraction with methylene chloride. Crystallization in ethyl acetate yields 520 mg of 6-iodo-4-methoxymethyl-beta-carboline-3-carboxylic-acid-ethylester with a m.p. of 204°-206° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04435403 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-4fbc0facc1c142b58a312c27b35df4b7 |
| Source note | uspto-grants-1984_03 |