HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967159Generated: November 1, 2026
N-Methylallylamine → HCID 178457227, compound
https://huagongshe.com/reaction/967159
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylallylamine | HCID 69391 | — |
| Reactant | HCID 178483634 | HCID 178483634 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 178457227 | HCID 178457227 | 65.5% |
Reaction Steps
A solution of 200 mg (0.43 mmol) trans-methanesulfonic acid 3-(4-{2-[methyl-(4-trifluoromethyl-phenoxycarbonyl)-amino]-ethyl}-cyclohexyl)-propyl ester and 0.204 ml (2.15 mmol) of allyl methyl amine in 2 ml of N,N-dimethylacetamide was stirred over night at 60° C. The reaction mixture was then taken up in ether and the ether phases were washed with water. The organic layer was dried over magnesium sulfate, concentrated under reduced pressure and the residue then chromatographed on silica gel with a 9:1 v/v mixture of dichloromethane and 1N ammonia in methanol as the eluent giving 124 mg (65.5%) trans-(2-{4-[3-(allyl-methyl-amino)-propyl]-cyclohexyl}-ethyl)-methyl-carbamic acid 4-trifluoromethyl-phenyl ester as colorless viscous oil, MS: 441 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06953806B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-9bcf3c439ff24ac49f13e0f0edc5910e |
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| Source note | uspto-grants-2005_10 |
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