HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648217Generated: October 30, 2026
Ethoxalyl chloride → HCID 20482445, compound
https://huagongshe.com/reaction/648217
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Reactant | HCID 13386489 | HCID 13386489 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20482445 | HCID 20482445 | 30.5% |
Reaction Steps
To a solution of 2-amino-4-(4-benzhydrylpiperazin-1-ylmethyl)thiazole (1.8 g) in tetrahydrofuran (5 ml) and pyridine (10 ml) was added dropwise ethoxalyl chloride (1.1 g) under ice-cooling with stirring, and the stirring was continued at the same temperature for an hour. After concentration of the reaction mixture, the residue was extracted with ethyl acetate, washed with water, dried over anhydrous magnesium sulfate and then evaporated to dryness to give a residue, which was chromatographed on silica gel using ethyl acetate as an eluent. The eluates containing the desired compound were collected and evaporated, followed by recrystallization from a mixture of ethyl acetate and n-hexane to obtain pale yellow crystals (0.7 g) of 4-(4-benzhydrylpiperazin-1-ylmethyl)-2-ethoxalylaminothiazole, mp 125°-128° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04411900 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-c3ee0f6a8d5e43fa9e28d946bc532670 |
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| Source note | uspto-grants-1983_10 |
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