HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108078Generated: October 31, 2026
Ammonium Bicarbonate → HCID 18786356, compound
https://huagongshe.com/reaction/1108078
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Bicarbonate | HCID 14013 | — |
| Reactant | 2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinoline | HCID 27833 | — |
| Reactant | HCID 18786346 | HCID 18786346 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18786356 | HCID 18786356 | 54.2% |
Reaction Steps
A suspension of 4-[3-[4-(pyrrol-1-ylmethyl)phenylthio]phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxylic acid (0.36 g, 0.93 mmol), ammonium bicarbonate (0.44 g, 5.58 mmol) and 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (0.28 g, 1.12 mmol) in dichloromethane (20 ml) were stirred at room temperature overnight. Ammonium bicarbonate and 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline were added until the acid was consumed. The reaction mixture was diluted with dichloromethane (50 ml) and washed with water (50 ml). The organic extract was washed with cold 1N hydrochloric acid (50 ml), water (50 ml) and saturated aqueous sodium bicarbonate (5 ml), water (50 ml) and brine (50 ml), dried (magnesium sulfate) and concentrated to dryness. Recrystallization of the residue from ethyl acetate afforded the titled compound (198 mg, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06063928 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-790f758284e04288adb9fa29e489ff43 |
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| Source note | uspto-grants-2000_05 |
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