HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082693Generated: November 1, 2026
HCID 20360439, compound → (5-Chloro-2-(3-(chloromethyl)-5-methyl-4H-1,2,4-triazol-4-yl)phenyl)(phenyl)methanone
https://huagongshe.com/reaction/2082693
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 20360439 | HCID 20360439 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | (5-Chloro-2-(3-(chloromethyl)-5-methyl-4H-1,2,4-triazol-4-yl)phenyl)(phenyl)methanone | HCID 21488575 | 86% |
Reaction Steps
A solution of 33 parts of 6-chloro-3-chloroacetylamino-3,4-dihydro-4-hydroxy-2-methyl-4-phenylquinazoline in 500 volume parts of formic acid is refluxed for 2.5 hours, followed by subjecting to distillation to remove the excess formic acid. The resulting residue is neutralized with a saturated aqueous solution of sodium bicarbonate, and extracted with ethylacetate. The ethyl acetate layer is washed with water and dried over sodium sulfate, followed by distilling off the solvent. The resulting product is recovered by filtration and washed with ether and then dried, whereby 5-chloro-2-(3-chloromethyl-5-methyl-s-triazol-4-yl) benzophenone are obtained as crystals. Recrystallization from acetoneether gives colorless granules melting at 140° to 142° C. Yield: 86%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04082764 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-0f91b915f57743ec9013c521f33fe033 |
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| Source note | uspto-grants-1978_04 |
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