HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564289Generated: October 31, 2026
Hydrochloric Acid → HCID 67005686, compound
https://huagongshe.com/reaction/564289
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 6-Aminobenzothiazole | HCID 68288 | — |
| Reactant | 3-Benzamidobenzoyl chloride | HCID 18470059 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67005686 | HCID 67005686 | 60.3% |
Reaction Steps
To a solution of 0.1 g of 6-aminobenzothiazole and 0.1 g of pyridine added to 5 ml of tetrahydrofuran and stirred at room temperature was introduced dropwise 0.2 g of 3-(benzoylamino)benzoyl chloride dissolved in 1 ml of tetrahydrofuran. The resulting solution was stirred at room temperature for 1 hour, and then ethyl acetate and 1N hydrochloric acid were added thereto for separating the organic phase. The organic phase was washed with saturated sodium hydrogen carbonate solution one time, and then dried over anhydrous magnesium sulfate. The solution was filtered off, the filtrate was collected, and the solvent was removed under a reduced pressure to obtain a residue. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=3:1) to obtain 0.15 g of the desired product (Yield: 52%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067638B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-7d742ced661e432cbf55e82b4c071c9f |
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| Source note | uspto-grants-2011_11 |
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