HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185483Generated: October 31, 2026
4-Methylmorpholine → 4-(3,5dichlorophenoxy)piperidine Dihydrochloride
https://huagongshe.com/reaction/2185483
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | n-Tert-butoxycarbonyl-trans-4-(n-tert-butoxycarbonylglycylamino)-d-proline | HCID 21341552 | — |
| Reactant | 4-(3,5-Dichlorophenoxy)piperidine | HCID 22458412 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(3,5dichlorophenoxy)piperidine Dihydrochloride | HCID 86758124 | 347.7% |
Reaction Steps
N-Methylmorpholine (70 μL) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (114 mg) were added to a solution of trans-4-(N-tert-butoxycarbonylglycylamino)-N-tert-butoxycarbonyl-D-proline (Compound D105 (F), 220 mg), 4-(3,5-dichlorophenoxy)piperidine (154 mg) and 1-hydroxybenzotriazole (85 mg) in tetrahydrofuran (8 mL) and N,N-dimethylformamide (2 mL) at room temperature. After stirring at room temperature for 12 hr, the reaction mixture was partitioned between ethyl acetate and 1 N hydrochloric acid. The organic layer was washed with saturated sodium hydrogen carbonate and brine. After drying over anhydrous sodium sulfate, the organic layer was evaporated in vacuo. The residue was washed with hexane to give the titled compound (347 mg) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06399629B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-e4bd081705494bc1983af18eb476ca84 |
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| Source note | uspto-grants-2002_06 |
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