HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 527955Erstellt: 26. Oktober 2026
6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-one → 6-[(S)-3-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-propylamino]-4H-benzo[1,4]oxazin-3-one
https://huagongshe.com/reaction/527955
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-one | HCID 2763681 | — |
| Edukt | (S)-Glycidoxy-t-butyldimethylsilane | HCID 10954307 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 6-[(S)-3-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-propylamino]-4H-benzo[1,4]oxazin-3-one | HCID 66737695 | 66,1% |
Reaktionsschritte
LiClO4 (7.20 g, 3 eq.) was added to a solution of tert-butyl-dimethyl-((S)-1-oxiranylmethoxy)-silane (commercial; 4.25 g, 22.6 mmol) in MeCN (70 mL). 6-amino-4H-benzo[1,4]oxazin-3-one (commercial; 3.70 g, 1 eq.) was then added and the mixture was stirred at 50° C. for 6 h. The solvent was removed under reduced pressure and the residue was purified by CC (DCM/MeOH/NH4OH 1000/25/2) to afford the title intermediate as a pale brown foam (5.25 g, 66% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09346804B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-f62c9553bde44f8aaa78ba59e9b288fd |
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| Quellennotiz | uspto-grants-2016_05 |
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