HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2387836Erstellt: 27. Oktober 2026
(S)-3-aminoheptan-1-ol → (S)-2-(4-((2-Amino-4-(1-hydroxyheptan-3-ylamino)-6-methylpyrimidin-5-yl)methyl)-3-fluorophenyl)acetonitrile
https://huagongshe.com/reaction/2387836
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | (S)-3-aminoheptan-1-ol | HCID 55290391 | — |
| Edukt | 2-(4-((2-Amino-4-chloro-6-methylpyrimidin-5-yl)methyl)-3-fluorophenyl)acetonitrile | HCID 86633405 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | (S)-2-(4-((2-Amino-4-(1-hydroxyheptan-3-ylamino)-6-methylpyrimidin-5-yl)methyl)-3-fluorophenyl)acetonitrile | HCID 68954091 | — |
Reaktionsschritte
(S)-3-Aminoheptan-1-ol (0.135 g) was added to a stirred solution of the product from step (iii) (0.12 g) in NMP (2 mL). The mixture was heated at 150° C. for 48 h, and then at 170° C. for a further 8 h. The mixture was allowed to cool, diluted with water (10 mL) and the aqueous extracted with EtOAc. The combined organic phase was dried and evaporated. The crude product was purified by column chromatography, to give the subtitle compound, 0.11 g.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08268990B2 |
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| Quelldatensatz | uspto-grants-2012_09 |
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| ORD ID | ord-ea1338bbcde34fa9a2c1eedde734fe03 |
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| Quellennotiz | uspto-grants-2012_09 |
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