HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → HCID 44125738, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 23133283 | HCID 23133283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 44125738 | HCID 44125738 | 37.6% |
Reaction Steps
Benzenesulfonyl chloride (48.6 mg, 0.28 mmol) was added to a solution of [3-(2,2a,4,5-Tetrahydro-1H-3-aza-acenaphthylen-3-yl)-propyl]-m-tolyl-amine dihydro-chloride (43.0 mg, 0.11 mmol) and N,N′-diisopropylethylamine (2 ml) in CH2Cl2 (2 mL) and the mixture was stirred overnight at room temperature. The resulting solution was washed with water (3×10 ml), dried over Na2SO4 and evaporated to dryness. The free base was dissolved in ethyl acetate (1 ml). A 2.8 M solution of hydrogen chloride in ethanol (0.10 mL) was then added. The product was crystallized and collected by filtration, and vacuum dried to give a white solid (20.0 mg, 36% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07662862B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-da2d649c4d854939b68652a57e7ca13f |
| Source note | uspto-grants-2010_02 |