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HRID 48521Erstellt: 23. Oktober 2026
Tetramethyltin → 5'-Methylspiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[2,3-b]pyridine]
https://huagongshe.com/de/reaction/48521
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetramethyltin | HCID 11661 | — |
| Edukt | Tri-o-tolylphosphine | HCID 80271 | — |
| Edukt | Lithium Chloride | HCID 433294 | — |
| Edukt | 5'-bromospiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[2,3-b]pyridine] | HCID 10357133 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Diglyme | HCID 8150 | — |
| Produkt | 5'-Methylspiro[1-azabicyclo[2.2.2]octane-3,2'(3'H)-furo[2,3-b]pyridine] | HCID 15908242 | 166,3% |
Reaktionsschritte
A solution containing 5′-bromospiro[1-azabicyclo[2.2.2]octane-3,2′(3′H)-furo[2,3-b]pyridine] (203 mg, 0.687 mmol), tris(dibenzylidineacetone)dipalladium (0) (33 mg, 0.036 mmol), tri(o-tolyl)phosphine (95 mg, 0.312 mmol), lithium chloride (241 mg, 5.69 mmol), and tetramethylstannane (1.0 ml, 1.3 g, 7.2 mmol) in 2-methoxyethyl ether (5 ml) was heated in a bath maintained at 100° C. After 3 h, a further portion of tetramethylstannane (1 ml, 1.3 g, 7.2 mmol) was added, and heating was continued overnight. The solution was filtered, and subjected to purification by HPLC using a gradient of 0-20% 1:1:2 7M methanolic ammonia:methanol:chloroform and chloroform to obtain the title compound (120 mg, 0.519 mmol, 76%) as a pale solid: electrospray MS (m/z, relative intensity) 231 ([MH]+, 100).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06703502B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-30448ba81ae5431491787ade7fb36520 |
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| Quellennotiz | uspto-grants-2004_03 |
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