HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735764Generated: October 30, 2026
Diethyl Pyrocarbonate → HCID 57847162, compound
https://huagongshe.com/reaction/735764
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Pyrocarbonate | HCID 3051 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (+)-cis-2-Benzamidocyclohexanecarboxylic Acid | HCID 1268229 | — |
| Reactant | HCID 57846949 | HCID 57846949 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57847162 | HCID 57847162 | 8% |
Reaction Steps
To a mixture of (3aS,4R*,9bR*)-3a-methyl-4-(3-thienyl)-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinoline (750 mg, 2.77 mmol), (1S,2R)-2-(benzoylamino)cyclohexanecarboxylic acid (685 mg, 2.77 mmol), triethylamine (606 mg, 6.10 mmol), acetonitrile (14 ml) and tetrahydrofuran (14 ml) was added DEPC (500 mg, 3.05 mmol) under ice-cooling, and the mixture was stirred for 10 min. The mixture was allowed to return to room temperature and stirred for 12 hrs. Saturated aqueous sodium hydrogen carbonate solution was added to the reaction mixture and the mixture was extracted with ethyl acetate. The extract was dried (over anhydrous Na2SO4), and the solvent was evaporated under reduced pressure. The residue was subjected to column chromatography using silica gel (100 g), and eluted with hexane-ethyl acetate (4:1-1:1, v/v) to give the title compound (3aR,4R,9bR) (110 mg, 8%) as an amorphous form from the first eluted fraction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592453B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-a184d02f53ed42118a5a9e8863636591 |
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| Source note | uspto-grants-2009_09 |
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