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HRID 1094975Erstellt: 26. Oktober 2026
Pyridine → 2-(3-Chloromethyl-benzoylamino)-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1094975
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Veratroyl chloride | HCID 77070 | — |
| Edukt | Ethyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate | HCID 78262 | — |
| Produkt | 2-(3-Chloromethyl-benzoylamino)-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid ethyl ester | HCID 66639201 | — |
Reaktionsschritte
2-Amino-4,5,6,7-tetrahydrobenzothiophene-3-carboxylic acid ethyl ester (Compound A) (4.0 g) was dissolved in anhydrous methylene chloride (40.0 ml). Subsequently, pyridine (2.8 ml) and 3-(chloromethyl)benzoyl chloride (compound B) (3.0 ml) were added at 0° C., and the mixture was stirred at 0° C. for one hr. After the completion of the reaction, distilled water was added, and the mixture was subjected to separatory extraction with chloroform, and the organic layer was washed with saturated brine, was dried over sodium sulfate, and was then concentrated to give 2-(3-chloromethyl-benzoylamino)-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid ethyl ester as a useful intermediate (7.42 g, yield 100%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08134015B2 |
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| Quelldatensatz | uspto-grants-2012_03 |
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| ORD ID | ord-d039a63894f94c38830b00a29956f7a9 |
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| Quellennotiz | uspto-grants-2012_03 |
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