HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550306Generated: October 29, 2026
Diethyl Pyrocarbonate → HCID 178495709, compound
https://huagongshe.com/reaction/550306
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Pyrocarbonate | HCID 3051 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (1R,2S)-2-{[(3aR,4R,9bR)-4-(methoxymethyl)-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinolin-1-yl]carbonyl}cyclohexaneamine hydrochloride | HCID 67150575 | — |
| Reactant | HCID 178524184 | HCID 178524184 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178495709 | HCID 178495709 | 80% |
Reaction Steps
To a solution (5 ml) of (1R,2S)-2-{[(3aR,4R,9bR)-4-(methoxymethyl)-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinolin-1-yl]carbonyl}cyclohexaneamine hydrochloride (200 mg, 0.480 mmol) in THF were added triethylamine (0.199 ml, 1.44 mmol), 1H-1,2,3-benzotriazole-5-carboxylic acid (78.3 mg, 0.480 mmol) and DEPC (0.079 ml, 0.528 mmol) under ice-cooling, and the mixture was stirred at room temperature for 1 hr. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous MgSO4, and concentrated under reduced pressure. The obtained residue was subjected to column chromatography using silica gel and eluted with hexane:ethyl acetate (1:1-1:9) to give the title compound (187 mg, 80%) as an amorphous form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943770B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-d6ba24cb92524e08b2a9b01469e564da |
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| Source note | uspto-grants-2011_05 |
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