HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420593Generated: October 26, 2026
Dimethylformamide → [3-[[[1-(6-Chlorobenzothiazole-2-yl)piperidine-4-yl]isopropylamino]methyl]phenyl]acetic acid methyl ester
https://huagongshe.com/reaction/420593
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3-Bromomethyl-phenyl)-acetic acid methyl ester | HCID 10014651 | — |
| Reactant | HCID 57966227 | HCID 57966227 | — |
| Solvent | Water | HCID 962 | — |
| Product | [3-[[[1-(6-Chlorobenzothiazole-2-yl)piperidine-4-yl]isopropylamino]methyl]phenyl]acetic acid methyl ester | HCID 57966261 | 37.2% |
Reaction Steps
A mixture of [1-(6-chlorobenzothiazole-2-yl)piperidine-4-yl]isopropylamine (159 mg), (3-bromomethylphenyl)acetic acid methyl ester (138 mg), potassium carbonate (107 mg) and dimethylformamide (2 mL) was stirred at 80° C. for 8 hours. To the reaction solution was added water and extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over magnesium sulphate. The solvent was evaporated under reduced pressure and the residue was purified by column chromatograph on silica gel to give the title compound (90 mg). Yield: 37%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097610B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-01c0932a77704c018ac6565d88b64913 |
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| Source note | uspto-grants-2012_01 |
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