HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525928Generated: October 28, 2026
1-Pyrrolidineethanamine → HCID 86732796, compound
https://huagongshe.com/reaction/525928
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Pyrrolidineethanamine | HCID 1344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | HCID 86732795 | HCID 86732795 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86732796 | HCID 86732796 | 33.8% |
Reaction Steps
To a suspension of 5-chloro-1-ethyl-6,7-bis((4-methoxybenzyl)oxy)-4-oxo-1,4-dihydrocinnoline-3-carboxylic acid (3 g, 5.71 mmol) in tetrahydrofuran (THF) (25 mL) was added triethylamine (0.876 mL, 6.29 mmol), followed by isobutyl chloroformate (0.826 mL, 6.29 mmol). The reaction mixture was stirred at 0° C. for 30 min. 2-(Pyrrolidin-1-yl)ethanamine (0.979 g, 8.57 mmol) was added and the mixture was stirred at 0° C. for 30 min and warmed up to room temperature for 2 h. Solvent was removed and the residue was chromatographed to afford 5-chloro-1-ethyl-6,7-bis((4-methoxybenzyl)oxy)-4-oxo-N-(2-(pyrrolidin-1-yl)ethyl)-1,4-dihydrocinnoline-3-carboxamide (1.2 g, 1.932 mmol, 33.8% yield). LCMS: (M+H)+: 621.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340556B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-a604e812734c430f9815b2988f7e8052 |
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| Source note | uspto-grants-2016_05 |
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