HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643157Generated: October 29, 2026
4-Nitrophenyl chloroformate → HCID 68676170, compound
https://huagongshe.com/reaction/643157
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitrophenyl chloroformate | HCID 82129 | — |
| Reactant | 3-(Piperidin-4-yl)quinolin-2(1H)-one | HCID 18321046 | — |
| Reactant | methyl(R)-3-(4-benzyloxy-3,5-dimethyl-phenyl)-2-hydroxy-propionate | HCID 67273374 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68676170 | HCID 68676170 | — |
Reaction Steps
Under a nitrogen atmosphere 0.91 g (4.38 mmol) 4-nitrophenyl chloroformate in 10 mL THF were metered into 20 mL pyridine within 10 min at a bath temperature of 60° C., the mixture was stirred for 10 min, then 1.38 g (4.38 mmol) methyl (R)-3-(4-benzyloxy-3,5-dimethyl-phenyl)-2-hydroxy-propionate in 40 mL pyridine were added and the reaction mixture was stirred for 2 h at 60° C. The reaction solution was combined with 1.00 g (4.38 mmol) 3-piperidin-4-yl-1H-quinoline-2-one and stirred for 4 h at 100° C. The reaction mixture was evaporated down i.vac. and the residue was purified by HPLC. The fractions containing the product were combined, evaporated down i.vac., the residue was made alkaline with 15% K2CO3 solution, the precipitate was suction filtered, washed with 20 mL water and dried at 50° C.
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-33b6433eecfa485e980b6ae881251536 |
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| Source note | uspto-grants-2010_04 |
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