HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127515Erstellt: 26. Oktober 2026
Methylamine → 4-Methylaminomethyl-2,3,4,9-tetrahydrothiopyrano[2,3-b]indole
https://huagongshe.com/reaction/127515
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methylamine | HCID 6329 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 4-Formyl-2,3,4,9-tetrahydrothiopyrano[2,3-b]indole | HCID 14735629 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 4-Methylaminomethyl-2,3,4,9-tetrahydrothiopyrano[2,3-b]indole | HCID 3056096 | 90% |
Reaktionsschritte
To a solution of the product of the above (2) (2.17 g) in absolute methanol (10 ml) is added a 30% solution (2.2 ml) of methylamine in methanol. The mixture is stirred at room temperature for 1 hour. Sodium borohydride (380 mg) is added to the filtrate. The mixture is stirred at room temperature for 2 hours and evaporated to remove the solvent. The residue is acidified with 2 N hydrochloric acid after addition of water. The solution is extracted with chloroform to remove neutral impurities. The aqueous layer is made alkaline with an aqueous solution of sodium hydroxide and extracted again with chloroform. The extract is washed with water, dried and evaporated to remove the solvent. The residue is treated with small amount of benzene to give the 1/6 benzene adduct (2.21 g) of the title compound melting at 78°-81° C. Yield: 90%
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04256640 |
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| Quelldatensatz | uspto-grants-1981_03 |
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| ORD ID | ord-7aefcbef30b7468589aab25cc4c62a5a |
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| Quellennotiz | uspto-grants-1981_03 |
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