HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N,N-Diallyl-N-({5-[(4-{3-[(trifluoromethyl)sulfonyl]anilino}piperidin-1-yl)sulfonyl]-thien-2-yl}methyl)amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(3-((trifluoromethyl)sulfonyl)phenyl)piperidin-4-amine | HCID 2776457 | — |
| Reactant | 5-Diallylaminomethyl-thiophene-2-sulfonyl chloride | HCID 11380769 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N,N-Diallyl-N-({5-[(4-{3-[(trifluoromethyl)sulfonyl]anilino}piperidin-1-yl)sulfonyl]-thien-2-yl}methyl)amine | HCID 86761398 | 86% |
Reaction Steps
A solution of 4-(3-trifluoromethanesulfonyl-phenylamino)-piperidine (731 mg, 237 mmol) and Et3N (0.5 mL, 3.58 mmol) in CH2Cl2 (20 mL) was treated with the diallylamino sulfonyl chloride 269b 23° C. A thick precipitate appeared within 5 min, and the mixture was stirred overnight (even if complete within minutes). Dilution with CH2Cl2 (50 mL), washing (1120; brine), drying (MgSO4), and evaporation afforded the crude product, which was filtered over silica gel (AcOEt:cyclohexane 1:1) to afford 1.15 g (86%) of the title bisallylamine, which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08012995B1 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-c77cbc0ec4854d71a1cc11b5f11eb2a0 |
| Source note | uspto-grants-2011_09 |