HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643153Generated: October 27, 2026
4-Nitrophenyl chloroformate → HCID 68676084, compound
https://huagongshe.com/reaction/643153
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | 3-Piperidin-4-yl-1,3-dihydroimidazo[4,5-c]quinolin-2-one | HCID 18321559 | — |
| Reactant | HCID 67273374 | HCID 67273374 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 68676084 | HCID 68676084 | — |
Reaction Steps
Under a nitrogen atmosphere 1.28 g (6.36 mmol) 4-nitrophenyl chloroformate were added at RT to a solution of 0.78 g (6.36 mmol) 4-dimethylaminopyridine in 100 mL pyridine and the mixture was stirred for 1 h at RT. Then a solution of 2.00 g (6.36 mmol) methyl (R)-3-(4-benzyloxy-3,5-dimethyl-phenyl)-2-hydroxy-propionate in 20 mL pyridine was added dropwise at RT and the reaction mixture was stirred for 2 h after the end of the addition. Then 1.71 g (6.36 mmol) 3-piperidin-4-yl-1,3-dihydro-imidazo[4,5-c]quinoline-2-one was added to the reaction mixture, which was then heated to 100° C. for 4 h. The precipitate formed was filtered off, the filtrate was evaporated down i.vac., the residue was mixed with 200 mL EtOAc and 200 mL semisaturated KHSO4 solution, the product being obtained as a precipitate. This was suction filtered and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696209B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-8b38c85137d74a43a2fc2a9d1393bcd4 |
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| Source note | uspto-grants-2010_04 |
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