HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → HCID 86615492, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 24897973 | HCID 24897973 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86615492 | HCID 86615492 | — |
Reaction Steps
The product from Example 6 (100 mg, 0.228 mmol) was reacted with methane sulfonyl chloride (28 mg, 0.251 mmol), N,N-diisopropylethylamine (88.4 mg, 0.684 mmol), and catalytic DMAP in CH2Cl2 for 18 h giving the crude title compound which was purified by HPLC with TFA providing the product as the trifluoroacetic acid (20 mg, 15%). 1H NMR (300 MHz, DMSO-d6) δ ppm: 0.97 (t, J=7.35 Hz, 3 H) 1.77-1.90 (m, 2 H) 2.40 (s, 3 H) 2.98 (t, J=7.54 Hz, 2 H) 3.43 (s, 3 H) 6.34 (d, J=6.99 Hz, 1 H) 7.19 (d, 2 H) 7.27 (d, 2 H) 7.36-7.40 (m, 2 H) 7.48 (d, 1 H) 7.78 (d, J=8.82 Hz, 1 H) 8.39 (d, J=6.99 Hz, 1 H) 8.91 (d, J=8.46 Hz, 1 H); MS (DCI NH3+) 480 m/z (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07763731B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-fcde19d45e2e419a9633284b658797e3 |
| Source note | uspto-grants-2010_07 |