HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521844Generated: October 30, 2026
Chloromethyl Methyl Ether → HCID 66580218, compound
https://huagongshe.com/reaction/1521844
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 66581050 | HCID 66581050 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66580218 | HCID 66580218 | — |
Reaction Steps
To a solution of 2-bromo-N-[3-(morpholin-4-ylcarbonyl)-1-phenyl-1H-pyrazol-4-yl]benzenesulfonamide (200 mg; 0.41 mmol; 1.00 eq.) in THF (30 mL) is added NaH (24 mg; 0.61 mmol; 1.50 eq.) in a portionwise manner and the resulting mixture is stirred at room temperature for 15 minutes whereupon Chloromethyl methyl ether (82 μl; 0.81 mmol; 2.00 eq.) is added dropwise. The reaction mixture is stirred at room temperature for 2 hours then quenched with sat. aq. NaHCO3. Extraction with ethyl acetate (2×), ishing with brine, drying over magnesium sulfate and concentration in vacuo gives 240 mg (quant) of the title compound as a colourless oil. 1H NMR (DMSO) δ 8.82 (s, 1H), 7.93-7.8 (m, 4H), 7.64-7.46 (m, 4H), 7.39 (t, J=7.4 Hz, 1H), 5.32 (s, 2H), 3.59-3.51 (m, 2H), 3.42 (s, 3H), 3.46-3.37 (m, 4H), 3.15-3.06 (m, 2H). MS (ESI+): 505.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09073940B2 |
|---|
| Source dataset | uspto-grants-2015_07 |
|---|
| ORD ID | ord-9f025f9eeb4a49c9b6457939c6af26d4 |
|---|
| Source note | uspto-grants-2015_07 |
|---|