HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434675Generated: October 25, 2026
Triethylamine → 2-Methyl-3-methylthio-4-morpholino-5-fluoro-7-bromoindole
https://huagongshe.com/reaction/434675
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tert-Butyl hypochlorite | HCID 521297 | — |
| Reactant | 1-Methylthio-2-propanone | HCID 6430713 | — |
| Reactant | 2-Bromo-4-fluoro-5-morpholinoaniline | HCID 20258977 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Methyl-3-methylthio-4-morpholino-5-fluoro-7-bromoindole | HCID 20258982 | 79.2% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04399134 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-3fa0a136cf90431dae32882b9896bbdb |
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| Source note | uspto-grants-1983_08 |
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