HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 434675Erstellt: 24. Oktober 2026
Triethylamine → 2-Methyl-3-methylthio-4-morpholino-5-fluoro-7-bromoindole
https://huagongshe.com/de/reaction/434675
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Tert-Butyl hypochlorite | HCID 521297 | — |
| Edukt | 1-Methylthio-2-propanone | HCID 6430713 | — |
| Edukt | 2-Bromo-4-fluoro-5-morpholinoaniline | HCID 20258977 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-Methyl-3-methylthio-4-morpholino-5-fluoro-7-bromoindole | HCID 20258982 | 79,2% |
Reaktionsschritte
A solution of 145 g of 2-bromo-4-fluoro-5-morpholinoaniline in 1 l of methylene chloride and the solution was cooled to a temperature of not higher than -50° C. on a dry ice-acetone bath. At the same temperature as above 60 g of tert-butyl hypochlorite was added dropwise to the solution during which operation the reaction system changed from heterogeneous mixture to homogeneous solution. Then, 67 g of methylthio-2-propanone was added dropwise to the solution and the mixture was reacted at the same temperature as above for 2 hours followed by adding dropwise 80 ml of triethylamine. After completion of addition, the temperature of the mixture was elevated slowly to room temperature. After room temperature was attained 1 l of water was added to separate the methylene chloride layer which then was dried over sodium sulfate and concentrated under reduced pressure to give 150 g of 2-methyl-3-methylthio-5-fluoro-4-morpholino-7-bromoindole.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04399134 |
|---|
| Quelldatensatz | uspto-grants-1983_08 |
|---|
| ORD ID | ord-3fa0a136cf90431dae32882b9896bbdb |
|---|
| Quellennotiz | uspto-grants-1983_08 |
|---|