HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573585Generated: October 30, 2026
Ethyl Acetoacetate → Ethyl 4-amino-6-methylthieno[2,3-b]pyridine-5-carboxylate
https://huagongshe.com/reaction/573585
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | 2-Aminothiophene-3-carbonitrile | HCID 736607 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 4-amino-6-methylthieno[2,3-b]pyridine-5-carboxylate | HCID 68323805 | — |
Reaction Steps
Alternatively, a mixture of 2-amino-3-thiophenecarbonitrile (2.5 g, 20.13 mmol), ethyl 3-oxobutanoate (2.80 mL, 22.15 mmol) and SnCl4 (4.73 mL, 40.3 mmol) in toluene (135 mL) was stirred at RT for 30 min, and then refluxed for 2 h. The mixture was then basified with 6M NaOH (ca. 25 mL), diluted with 10% MeOH in DCM (40 mL), and the mixture filtered through celite. The organic layer of the filtrate was then separated and the aqueous layer re-extracted with 10% MeOH in DCM (50 mL×3). The combined organic layers were dried and concentrated. The residue was then purified by chromatography on silica, eluting with a gradient of 0-10% ethyl acetate in DCM, to give the title compound. Another batch of 2-amino-3-thiophenecarbonitrile (2.5 g, 20.13 mmol) was subjected to the same procedure and the products from each reaction were combined to give the title compound (2.36 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029545B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-276dbf979b2348b1874b6a09f80016cd |
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| Source note | uspto-grants-2015_05 |
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