HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → HCID 68577068, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Reactant | HCID 59254992 | HCID 59254992 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68577068 | HCID 68577068 | 82% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of compound 31 (5 mg, 0.012 mmol) in dry CH2Cl2 (0.2 mL) was added 4 M HCl dioxane solution (0.5 mL) and stirred for 2 h at 0° C. The solvent was evaporated under reduced pressure. The crude amine salt 32 was dissolved in CH2Cl2 (0.5 mL) and slowly added methanesulfonyl chloride (2 μL, 0.030 mmol) and TEA (9 μL, 0.064 mmol) at 0° C. After 1 h stirring, the reaction mixture was concentrated under reduced pressure. The crude product was purified on a silica gel column chromatography (3:1 n-Hexane/EtOAc) to give a colorless oil (3 mg, 82% yield): 1H NMR (300 MHz, CDCl3) 1.08˜1.87 (m, 20H); 2.36 (d, J=12.4 Hz, 1H); 2.77˜2.92 (m, 5H); 3.51˜3.54 (m, 1H); 4.10˜4.15 (m, 1H); 6.86˜6.96 (m, 2H); 7.13 (d, J=8.3 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07691874B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-b210b5eeec3942e0bedd00958cdf4bdb |
| Source note | uspto-grants-2010_04 |