HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 46317Erstellt: 23. Oktober 2026
1,3,4-Thiadiazol-2-amine → N-(2,4-dimethoxybenzyl)-1,3,4-thiadiazol-2-amine
https://huagongshe.com/de/reaction/46317
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,3,4-Thiadiazol-2-amine | HCID 19909 | — |
| Edukt | 2,4-Dimethoxybenzaldehyde | HCID 69175 | — |
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Katalysator | HCID 178460663 | HCID 178460663 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-(2,4-dimethoxybenzyl)-1,3,4-thiadiazol-2-amine | HCID 58042278 | 45% |
Reaktionsschritte
To a solution of 2-amino-1,3,4-thiadiazole (3.05 g, 0.0302 mol) and 2,4-dimethoxy-benzaldehyde (4.55 g, 0.0274 mol) in dichloromethane (125 mL) was added chlorotriisopropoxytitanium (16 mL, 0.067 mol) portionwise over 5 minutes. After stirring for 1 hour, sodium triacetoxyborohydride (11.72 g, 0.05530 mol) was added portion wise and stirred for 24 hours. The reaction was quenched with saturated aqueous sodium bicarbonate solution and adjusted to pH 9 with sodium hydroxide (6 N aqueous solution) and extracted with dichloromethane. The combined organic extracts were dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography eluting with methanol:dichloromethane (gradient 0:1 to 1:9, by volume) to afford the title compound as a white solid, 590 mg, 45% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541588B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-015316899b3a4942a482a9e33c8ef297 |
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| Quellennotiz | uspto-grants-2013_09 |
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