HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743080Generated: October 30, 2026
3-Thiophenecarboxaldehyde → HCID 19423540, compound
https://huagongshe.com/reaction/743080
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Thiophenecarboxaldehyde | HCID 68135 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 19423601 | HCID 19423601 | — |
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19423540 | HCID 19423540 | 84% |
Reaction Steps
To a solution of 500 mg (1.62 mmol) of 3-(piperidin-4-yl)-4-phenyl-2-oxo-1,2,3,4-tetrahydropyrido[4,3-d]pyrimidine in 30 mL of methanol were added 1,200 mg of 10% HCl/ethanol solution, 727 mg (6.48 mmol) of 3-thiophenecarboxaldehyde and 407 mg (6.48 mmol) of sodium cyanoborohydride under ice-cooling, and the mixture was stirred for 10 hours at ambient temperature. Then, the reaction mixture was concentrated in vacuo, and water was added to the residue. The mixture was adjusted to pH 10 and extracted with chloroform. The organic layer separated was dried on potassium carbonate, and then concentrated in vacuo. The residue was purified by means of column chromatography (silica gel, 1:9 methanol:chloroform) to give 550 mg (1.36 mmol) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05556860 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-8cb4df1b4eec469592f85fb925a0f28c |
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| Source note | uspto-grants-1996_09 |
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