HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1951093Generated: November 3, 2026
Diisopropylethylamine → HCID 68953198, compound
https://huagongshe.com/reaction/1951093
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Methoxy-3-(trifluoromethyl)benzoyl chloride | HCID 2775298 | — |
| Reactant | [(3SR,4RS)-3-(3,4-Dichloro-phenyl)-4-methylamino-pyrrolidin-1-yl]-[1-(1-methyl-cyclopropanecarbonyl)-piperidin-4-yl]-methanone | HCID 67025815 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68953198 | HCID 68953198 | 79% |
Reaction Steps
To a solution of {4-[(3SR,4RS)-3-(3,4-dichloro-phenyl)-4-methylamino-pyrrolidine-1-carbonyl]-piperidin-1-yl}-(1-methyl-cyclopropyl)-methanone (200 mg, 0.456 mmol) in THF (2 mL) was added N,N-diisopropyl ethyl amine (117 μl, 0.684 mmol), 4-methoxy-3-(trifluoromethyl)benzoyl chloride (131 mg, 0.547 mmol) and stirred for 4 h at ambient temperature. The reaction mixture was diluted with ethzl acetatec (10 mL) and was washed with an aqueous solution of sodium carbonate (1 M, 10 mL), water (10 mL) and brine (10 mL). The aqueous layers were extracted with ethyl acetate (20 mL) and the combined organic layers were dried over sodium sulfate. Purification by chromatography (SiO2, heptane:ethyl acetate:methanol=50:50:0 to 0:90:10) afforded the title compound (230 mg, 79%) as a colorless oil. MS m/e: 640.3 [M]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404679B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-1bc3cef57f794e2e816f7d0f5229139d |
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| Source note | uspto-grants-2013_03 |
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