HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706974Generated: November 2, 2026
1-Methylpiperazine → HCID 53680343, compound
https://huagongshe.com/reaction/1706974
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 54482160 | HCID 54482160 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 53680343 | HCID 53680343 | — |
Reaction Steps
A mixture of 8.0 g (0.015 mole) of 1-[2-(o-chlorobenzoyl)-4-chlorophenyl]-5-(iodomethyl)-1H-1,2,4-triazole-3-carboxylic acid methyl ester [see Example 13(b)] and 3.3 ml of 1-methyl-piperazine in 160 ml of methanol is stirred for 16 hours at 40°. The reaction solution is then concentrated in vacuo; water is added to the residue and extraction is performed twice with methylene chloride. The organic phase is washed twice with ice water, and extraction is then performed twice with 2 N hydrochloric acid solution. To the aqueous acidified extracts there are added ice and sufficient 5 N sodium hydroxide solution to bring the pH-value to 10. The base that has precipitated is taken up in ether. The organic phase is washed twice with saturated sodium chloride solution; it is afterwards dried over sodium sulphate and concentrated in vacuo to dryness. There is obtained 1-[2-(o-chlorobenzoyl)-4-chlorophenyl]-5-[(4-methyl-1-piperazinyl)-methyl]-1H-1,2,4-triazole-3-carboxylic acid methyl ester as solidified foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04209515 |
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| Source dataset | uspto-grants-1980_06 |
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| ORD ID | ord-34a74d2e9c5441c8bfc85f34b780fb09 |
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| Source note | uspto-grants-1980_06 |
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