HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167549Generated: October 28, 2026
Hydrochloric Acid → HCID 131723414, compound
https://huagongshe.com/reaction/1167549
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 178452276 | HCID 178452276 | — |
| Product | HCID 131723414 | HCID 131723414 | 90% |
Reaction Steps
A solution of HCl in methanol (5 mL) was generated by addition of acetyl chloride (200 mg) to methanol while cooling (5° C.). 3-(4-Chlorophenyl)-4-(4-pyridyl)-5-(4-N-tert.-butoxycarbonylpiperazinyl)pyrazole (100 mg, 0.2 mmol) prepared above was added and the reaction stirred in the cold for one hour. The reaction mixture was concentrated in vacuo and the residue azeotroped with toluene to give 100 mg of 1-[5-(4-chlorophenyl)-4-(4-pyridinyl)-1-(2-propynyl)-1H-pyrazol-3-yl]piperazine, trihydrochloride monohydrate (90%), m.p.=231-233° C. (dec.). Anal. Calc'd. for C21H20N5Cl.3HCl.H2O: C, 49.92; H, 4.99; N, 13.86. Found: C, 49.71; H, 4.89; N, 13.61.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06617324B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-df2d53a1e8104bf1ac656807d43f832c |
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| Source note | uspto-grants-2003_09 |
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