HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820191Generated: October 30, 2026
Diisopropylethylamine → HCID 57888738, compound
https://huagongshe.com/reaction/1820191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-(Chloromethyl)benzoyl chloride | HCID 2733324 | — |
| Reactant | HCID 67299489 | HCID 67299489 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57888738 | HCID 57888738 | 58% |
Reaction Steps
To a solution of (R)-2-Amino-1-(4-(4-chlorophenyl)piperidin-1-yl)-3-methylbutan-1-one hydrochloride (30.5 mg, 0.092 mmol) in DCM (1 mL) cooled to 0° C. was added DIEA (17.4 μL, 0.1 mmol) followed by 3-chloromethyl benzoylchloride (14.2 μL, 0.1 mmol). Upon completion of addition, the reaction mixture was allowed to warm slowly to rt. where it stirred overnight. After this time, the solution was diluted with dichloromethane and quenched by the addition of aqueous NaHCO3. The layers were separated and the organic layer was dried over Na2SO4, filtered, and concentrated to yield a residue. The residue was purified via SiO2 chromatography to give the (R)-3-(chloromethyl)-N-(1-(4-(4-chlorophenyl)piperidin-1-yl)-3-methyl-1-oxobutan-2-yl)benzamide as a clear glassy solid (23.7 mg, 58% yield). MS found: 447.3 (M+), 449.3 (M+2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601844B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-602223f1d4d4492a9b4458266ff2e17d |
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| Source note | uspto-grants-2009_10 |
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