HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 87545978, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Bromo-2-(trifluoromethyl)benzenesulfonyl chloride | HCID 2778608 | — |
| Reactant | HCID 68717531 | HCID 68717531 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 87545978 | HCID 87545978 | — |
Reaction Steps
DMF (1 ml) was added to a vial containing 4-(Azetidin-1-ylmethyl)-1H-indole (10 mg, 0.054 mmol; Intermediate 77) and 60% NaH (5.4 mg, 0.13 mmol) at rt. The mixture was stirred for 20 minutes before 4-bromo-2-(trifluoromethyl)benzenesulphonyl chloride (24.2 mg, 0.11 mmol) was added. The mixture was allowed to stir for 1 hour and 2 drops of 1N HCl was added. The mixture was diluted with MeOH, filtered and purified using preparative HPLC with ACE C8 5 μm (21.2×100 mm) column. Water containing 0.1% TFA and acetonitrile were used as mobile phases at a flow rate of 20 ml/min with gradient times of 11.5 min. Yield: 11 mg (35%). Light brown liquid. MS (ESI+) for C19H16BrF3N2O2S m/z 475 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07812017B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-446008ef2bd84defbefdecb3a2ca2b61 |
| Source note | uspto-grants-2010_10 |