HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 60459Erstellt: 24. Oktober 2026
6-bromo-5-((4-chlorophenyl)(hydroxy)methyl)-1-methyl-3-(3-((tetrahydro-2H-pyran-2-yl)oxy)propyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione → 3-(6-bromo-5-(4-chlorobenzyl)-1-methyl-2,4-dioxo-1,2-dihydropyrido[2,3-d]pyrimidin-3(4H)-yl)propyl formate
https://huagongshe.com/de/reaction/60459
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 6-bromo-5-((4-chlorophenyl)(hydroxy)methyl)-1-methyl-3-(3-((tetrahydro-2H-pyran-2-yl)oxy)propyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione | HCID 118875511 | — |
| Katalysator | Zinc | HCID 23994 | — |
| Lösungsmittel | Formic Acid | HCID 284 | — |
| Produkt | 3-(6-bromo-5-(4-chlorobenzyl)-1-methyl-2,4-dioxo-1,2-dihydropyrido[2,3-d]pyrimidin-3(4H)-yl)propyl formate | HCID 118875889 | 10% |
Reaktionsschritte
To a solution of 6-bromo-5-((4-chlorophenyl)(hydroxy)methyl)-1-methyl-3-(3-(tetrahydro-2H-pyran-2-yloxy)propyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione (800 mg, 1.50 mmol) in HCOOH (10 mL) was added Zn dust (484 mg, 7.50 mmol). The reaction was heated at 60° C. for 2 h cooled to RT and filtered. The filtrate was concentrated to give 3-(6-bromo-5-(4-chlorobenzyl)-1-methyl-2,4-dioxo-1,2-dihydropyrido[2,3-d]pyrimidin-3(4H)-yl)propyl formate (70 mg, 10% yield) as an oil. LCMS: MH+ 466 and TR=1.753 min. Used without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09440972B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-936ce9997ba7433984e41318f5bcb48b |
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| Quellennotiz | uspto-grants-2016_09 |
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