HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301114Generated: November 2, 2026
5-(tert-Butoxycarbonyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine-2-carboxylic acid → HCID 18377335, compound
https://huagongshe.com/reaction/2301114
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-(tert-Butoxycarbonyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine-2-carboxylic acid | HCID 17750399 | — |
| Reactant | Ammonia dioxane | HCID 66648793 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18377335 | HCID 18377335 | — |
Reaction Steps
5-t-Butoxycarbonyl-4,5,6,7-tetrahydro-thieno[3,2-c]pyridine-2-carboxylic acid (570 mg, 2.0 mmol) was dissolved in anhydrous tetrahydrofuran (10 ml), and the solution was mixed with 1,1-carbonyldiimidazole (320 mg, 2.0 mmol) and stirred at room temperature for 1 hour. The reaction solution was mixed with ammonia dioxane solution (0.5 M, 8.0 ml, 4.0 mmol) and the stirring was continued for 16 hours. The solvent was removed by evaporation from the reaction solution under a reduced pressure, and the residue was mixed with ethyl acetate and washed with water, hydrochloric acid (1 N), sodium hydroxide aqueous solution (1 N) and saturated brine. The organic layer was dried with anhydrous sodium sulfate, and the solvent was removed by evaporation under a reduced pressure to obtain 450 mg (1.6 mmol, 80% in yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06498251B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-879ceb0bf5ac4a16aba5a33d56be8123 |
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| Source note | uspto-grants-2002_12 |
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