HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925317Generated: October 28, 2026
4-Chlorobenzoyl chloride → HCID 59813633, compound
https://huagongshe.com/reaction/1925317
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 67520515 | HCID 67520515 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59813633 | HCID 59813633 | — |
Reaction Steps
To a solution of 7-(6,7-dimethoxyquinolin-4-yloxy)naphthalen-2-amine (0.110 g, 0.31 mmol) in 10 ml of CH2Cl2 was added K2CO3 (0.086 g, 0.62 mmol). The mixture was cooled to 0° C. and 4-chlorobenzoyl chloride (44 mL, 0.34 mmol) was added. The solution was stirred for 16 h and allowed to gradually warm up to RT. The reaction was diluted with water and extracted with EtOAc 3×. The organic layer was dried (Na2SO4), filtered and concentrated. The residue was purified using a Gilson Prep HPLC system. The fractions were collected, combined, and extracted with EtOAc 3×. The organic layer was dried (Na2SO4), filtered and concentrated to afford the desired compound. MS (ESI, pos. ion) m/z: 485.0 (M+1). Mass Calc'd for C29H21ClN2O4: 484.937.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178557B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-497068b3307b4568a2d8c95de1f11bd0 |
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| Source note | uspto-grants-2012_05 |
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