HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256823Generated: October 31, 2026
HCID 19784284, compound → HCID 19784266, compound
https://huagongshe.com/reaction/256823
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 19784284 | HCID 19784284 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | HCID 19784266 | HCID 19784266 | 99.3% |
Reaction Steps
3-[3-(4-Phenyl-1-piperazinyl)propyl]-2-trifluoroacetylimino-6-trifluoromethoxybenzothiazoline hydrochloride (3.6 g), dissolved in a mixture of 7% strength aqueous potassium carbonate solution (45 cc) and methanol (150 cc), is stirred for 4 hours at a temperature in the region of 20° C. After concentration to dryness, the reaction medium is taken up in distilled water (100 cc) and the organic phase extracted with ethyl acetate (2×100 cc), dried over magnesium sulphate and concentrated to dryness under reduced pressure (20 mmHg; 2.7 kPa). After formation of the dihydrochloride by adding 4.2N ethereal hydrogen chloride (4 cc) in ethyl acetate, the precipitate is recrystallized in an absolute ethanol/ethyl ether mixture (50:50 by volume). 2-Imino-3-[3-(4-phenyl-1-piperazinyl)propyl]-6-trifluoromethoxybenzothiazoline dihydrochloride (1.6 g), m.p. 260° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05260297 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-61d5359b527d4aaaa3e8057f3e57dc5b |
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| Source note | uspto-grants-1993_11 |
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