HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175816Generated: November 1, 2026
Chloroacetyl chloride → HCID 135600033, compound
https://huagongshe.com/reaction/1175816
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 135599894 | HCID 135599894 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 135600033 | HCID 135600033 | — |
Reaction Steps
A mixture of 3,7-diamino-2-phenyl-2,5-dihydro-4H-pyrazolo[4,3-c]quinolin-4-one (100 mg), chloroacetyl chloride (28.6 μl), triethylamine (71.7 μl ) and tetrahydrofuran (6 ml) was stirred at room temperature for 30 minutes, and 1-methylpiperazine (76.1 μl) was added thereto. The reaction mixture was stirred at room temperature for additional 30 minutes and with heating under reflux for 6 hours. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The extract was washed with water and brine, dried over anhydrous magnesium sulfate and then the solvent was distilled off under reduced pressure. Ethyl acetate was added to the residue. The precipitated solid was collected by filtration, and washed with ethyl acetate to obtain the target compound (64 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842701B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-0bfd633227f440f9972bc86a8adf0c34 |
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| Source note | uspto-grants-2010_11 |
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