HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 453376Erstellt: 23. Oktober 2026
Diisopropylamine → 2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamide
https://huagongshe.com/de/reaction/453376
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylamine | HCID 7912 | — |
| Edukt | Pyrimidin-5-amine | HCID 344373 | — |
| Edukt | 2-Methyl-5-nitrobenzoic acid | HCID 519683 | — |
| Edukt | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamide | HCID 24823255 | — |
Reaktionsschritte
In a 2L round bottom flask with mechanical stirring was charged with 2-methyl-5-nitrobenzoic acid (20 g), HATU (38 g) and diisopropylamine (32 mL) in DMF (90 mL). This mixture was stirred for 30 min then pyrimidin-5-amine was added and the reaction was stirred for 18 hr. The LCMS showed complete conversion. DMF was removed under vacuum as much as possible then water was added and a solid precipitated out (use mechanical stirring). The tan solid was filtered and rinsed with water, then taken up in EtOAc, washed with brine, dried over MgSO4, filtered and concentrated down. The crude was taken up in EtOAc and the product 45 precipitated out. This was filtered and the filtrate was concentrated down and taken up in EtOAc/Hex. After standing overnight, more solids were filtered and were combined with the first crop. 2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamide 45 was obtained as a light yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08492404B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-8412d5d5f20e47908513066372e957b3 |
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| Quellennotiz | uspto-grants-2013_07 |
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