Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 86681546 | HCID 86681546 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 71522298 | HCID 71522298 | — |
Reaction Steps
To a solution of 1-(cyclohexyl(methyl)amino)propan-2-yl 4-isopropylbenzoate (0.5 g, 1.57 mmol) in DCE (5 mL, methyl iodide (0.2 mL, 3.15 mmol) was added. The resultant reaction mixture was stirred at rt for 16 hours. The solvent was evaporated, and the crude product was purified by column chromatography. The product isolated was re-crystallized from methanol/ether. Yield: 134.9 mg (18.65%). 1H NMR (400 MHz, DMSO-d6) δ 7.94-7.92 (d, J=8 Hz, 2H), 7.43-7.41 (d, J=8 Hz, 2H), 5.54-5.50 (m, 1H), 3.95-3.89 (m, 1H), 3.61-3.58 (d, J=14 Hz, 1H), 3.40-3.34 (m, 1H), 3.03-2.95 (m, 7H), 2.22-2.20 (d, J=11 Hz, 1H), 2.10-2.07 (d, J=11 Hz, 1H), 1.86-1.83 (m, 2H), 1.57-1.43 (m, 3H), 1.36-1.35 (d, J=6 Hz, 3H), 1.16-1.11 (m, 9H). LCMS: m/z=331.8 [M+], RT=3.08 min (Column: Y, Program: P1). UPLC: 99.65% (200 nm), RT 3.09 min (Mobile phase: A. ACN, B. 0.05% HCOOH in water, Column: Gemini® NX C18 (50*4.6 mm) 3μ.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09180115B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-07315f7b60304ec2b41b7d119418e027 |
|---|
| Source note | uspto-grants-2015_11 |
|---|