HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 970424Erstellt: 26. Oktober 2026
Tert-Butylamine → 2,4-Dichloro-pyrimidine-5-carboxylic acid-tert-butylamide
https://huagongshe.com/reaction/970424
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Tert-Butylamine | HCID 6385 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2,4-Dichloropyrimidine-5-carbonyl chloride | HCID 13784112 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2,4-Dichloro-pyrimidine-5-carboxylic acid-tert-butylamide | HCID 22326752 | — |
Reaktionsschritte
A solution of 24.85 g (117.5 mmol) of 2,4-dichloro-pyrimidine-5-carbonyl chloride in 125 ml of THF is cooled to −15° C. It is slowly mixed with a solution of 13.2 ml (124.5 mmol) of tert-buylamine and 17.4 ml (125.7 mmol) of triethylamine in 50 ml of THF, so that the temperature of the reaction mixture remains less than −10° C. It is stirred for another 2 hours at −10° C., then the cooling bath is removed, and the reaction mixture is heated to room temperature while being stirred. After 1 hour, the precipitate that is formed is filtered off, and the filtrate is completely concentrated by evaporation. The residue that is obtained is purified by chromatography (hexane/ethyl acetate 4:1). 14.01 g (56.6 mmol, corresponding to 50% of theory) of the product is obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07312225B2 |
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| Quelldatensatz | uspto-grants-2007_12 |
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| ORD ID | ord-c9ce549a9b4a400299e4e4993e01a424 |
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| Quellennotiz | uspto-grants-2007_12 |
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