HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711606Generated: October 25, 2026
Sodium Hydroxide → HCID 178435039, compound
https://huagongshe.com/reaction/711606
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(3-cyano-4,5-dimethylthiophen-2-ylcarbamoyl)benzamide | HCID 57456902 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178435039 | HCID 178435039 | 96% |
Reaction Steps
A solution of N-(3-cyano-4,5-dimethylthiophen-2-ylcarbamoyl)benzamide (example 4a) (44.35 g, 148.1 mmol) and NaOH (2 N, 204 mL) in EtOH (400 mL) was stirred at 100° C. under nitrogen for four hours. The clear reaction solution was filtered and the filtrate was cooling to room temperature, and then was carefully neutralized with 10% AcOH (˜120 mL) with vigorous stirring at 0° C. After stirring overnight from 0° C. to room temperature, the resultant precipitate was collected by filtration, washed with warm water (60-70° C., 150 mL×4) and 20% EtOH in water (200 mL×2), and then dried at 50° C. under vacuum overnight to give the final product 4-amino-5,6-dimethylthieno[2,3-d]pyrimidin-2(1H)-one (27.7 g, 96%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 7.98 (brs, 1H), 2.24 (s, 3H), 2.19 (s, 3H). MS 196 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181276B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-4231b8b8d50446a191f8aa22502c1986 |
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| Source note | uspto-grants-2015_11 |
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