HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217269Generated: November 3, 2026
Trifluoroacetic acid → HCID 17958697, compound
https://huagongshe.com/reaction/2217269
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 17958696 | HCID 17958696 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 17958697 | HCID 17958697 | — |
Reaction Steps
2 mL of trifluoroacetic acid were added to the ice-cooled solution of 1.1 g (2.561 mmol) of 3,4-dihydro-3-[1-(1,1-dimethylethoxycarbonyl)-4-piperidinyl]-6-(4-methyl-1-piperazinyl)-2(1H)-quinazolinone in 20 mL of methylene chloride. The reaction mixture was stirred for 15 hours at ambient temperature and for 5 hours at 40° C. and then evaporated down in vacuo. The residue remaining was taken up in 5 mL of water, the solution formed was saturated with potassium carbonate and extracted exhaustively with dichloromethane. The combined extracts were evaporated down in vacuo. The residue obtained was purified by column chromatography on silica gel using dichloromethane/methanol 9/1 (v/v) to start with, then dichloromethane/methanol/concentrated ammonia 70/30/3 (v/v/v) as eluant. The appropriate fractions were evaporated down in vacuo, the residue remaining (0.5 g; 59% of theoretical) was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07407963B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-00f03940d88d4d19903f8bc62e802cc8 |
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| Source note | uspto-grants-2008_08 |
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