HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691983Generated: October 30, 2026
Diisopropylethylamine → HCID 66906271, compound
https://huagongshe.com/reaction/1691983
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Bromo-2-chlorobenzothiazole | HCID 2049871 | — |
| Reactant | (3S)-Piperidin-3-ol--hydrogen chloride (1/1) | HCID 16211918 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 66906271 | HCID 66906271 | — |
Reaction Steps
A mixture of 6-bromo-2-chlorobenzo[d]thiazole (1.0 g, 4.0 mmol) and (S)-piperidin-3-ol hydrochloride (0.609 g, 4.43 mmol), and N,N-diisopropylethylamine (3.51 mL, 0.02012 mole) in N,N-dimethylformamide (2.0 mL) was heated to 150° C. under microwave irradiation for 15 minutes. The reaction mixture was transferred to a 100 mL round bottom flask (methanol rinse) and volatiles were removed under reduced pressure. The residue was partitioned between CHCl3 and saturated aqueous sodium carbonate. The organic layer was dried over MgSO4. Drying agent was removed by filtration and the filtrate was concentrated under reduced pressure. The crude material was purified by column chromatography on an Analogix IntelliFlash-280 (Analogix SF15-12g, 100% CHCl3 to 60:40 CHCl3/ethyl acetate). Fractions containing product were combined and concentrated under reduced pressure to provide (S)-1-(6-bromobenzo[d]thiazol-2-yl)piperidin-3-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153813B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-77ae1a62860e484d827f9324d2870241 |
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| Source note | uspto-grants-2012_04 |
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