HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230683Generated: October 30, 2026
N,N-Dimethylglycine → 4-Morpholinyl{4-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methanone
https://huagongshe.com/reaction/230683
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylglycine | HCID 673 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-[(4-Iodophenyl)carbonyl]morpholine | HCID 772634 | — |
| Reactant | 3-(Trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole | HCID 2802863 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-Morpholinyl{4-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methanone | HCID 1316629 | 82% |
Reaction Steps
A mixture of 4-[(4-iodophenyl)carbonyl]morpholine (1.90 g, 6.0 mmol), 3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole (1.14 g, 6.0 mmol), copper (I) oxide (10 mol %, 0.6 mmol, 86 mg), N,N-dimethylglycine (20 mol %, 1.2 mmol, 124 mg), and cesium carbonate (12.0 mmol, 3.91 g) in dimethylsulfoxide (16 ml) was stirred in an oilbath heated at 130° C. for 24 h under argon and then allowed to cool to room temperature. The reaction mixture was partitioned between dichloromethane (30 ml) and water (30 ml). The organic layer was separated and dried over sodium sulphate. The solvent was removed by rotary evaporation to give a dark brown residue that was added to a 20 g isolute pre-packed silica column and eluted from 0-50% ethyl acetate in petroleum ether to give the title compound as a brown gum (1.86 g, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07566735B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-6ad4561296a5482eb86433f37de142e2 |
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| Source note | uspto-grants-2009_07 |
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