HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412302Generated: October 29, 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 22258799, compound
https://huagongshe.com/reaction/412302
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Triethyl 2-fluoro-2-phosphonoacetate | HCID 2734865 | — |
| Reactant | HCID 22258763 | HCID 22258763 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22258799 | HCID 22258799 | — |
Reaction Steps
To a stirred solution of tert-butyl 3-(2-amino-6-{2-(cyclopropylmethoxy)-6-[(4-methoxybenzyl)oxy]phenyl}-3-formyl-4-pyridinyl)-1-piperidinecarboxylate (0.500 g, 5 0.851 mmol), triethyl-2-fluoro-2-phosphonoacetate (0.350 mL, 1.701 mmol) and anhydrous lithium chloride (0.072 g, 1.701 mmol) in acetonitrile (20 mL) was added 1,8-diazabicyclo[5,4,0]undec-7-ene (0.250 mL, 1.701 mmol). The mixture was stirred at room temperature for 30 min and concentrated under reduced pressure. The residue was extracted with ethyl acetate and water. The separated organic phase was washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The resulting residue (liquid) was purified by column chromatography on silica gel (hexane/ethyl acetate=2/1-1/1) to give tert-butyl 3-(2-{2-(cyclopropylmethoxy)-6-[(4-methoxybenzyl)oxy]phenyl}-6-fluoro-7-oxo-7,8-dihydro-1,8-naphthyridin-4-yl)-1-piperidinecarboxylate as a form (0.261 g, 49%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06562811B1 |
|---|
| Source dataset | uspto-grants-2003_05 |
|---|
| ORD ID | ord-0ad92a8be48c4ab9af53e7b493c7c452 |
|---|
| Source note | uspto-grants-2003_05 |
|---|