HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928514Generated: November 1, 2026
Diisopropylethylamine → N-(2-Methoxy-acetyl)-3-[6'-methyl-4'-(4-trifluoromethyl-phenyl)-[2,2']bipyridinyl-6-yl]-benzenesulfonamide
https://huagongshe.com/reaction/1928514
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methoxyacetyl chloride | HCID 96623 | — |
| Reactant | 3-[6'-Methyl-4'-(4-trifluoromethyl-phenyl)-[2,2']bipyridinyl-6-yl]-benzenesulfonamide | HCID 24760738 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-Methoxy-acetyl)-3-[6'-methyl-4'-(4-trifluoromethyl-phenyl)-[2,2']bipyridinyl-6-yl]-benzenesulfonamide | HCID 68696917 | 13.3% |
Reaction Steps
A mixture of 3-[6′-methyl-4′-(4-trifluoromethyl-phenyl)-[2,2′]bipyridinyl-6-yl]-benzenesulfonamide (example 266) (300 mg, 0.639 mmol), N-ethyldiisopropylamine (0.22 ml, 1.278 mmol) and methoxyacetyl chloride (0.067 ml, 0.639 mmol) in dichloromethane (3 ml) was stirred at 23° C. for 16 h. Diluted with dichloromethane, washed with water, dried the organic layer over MgSO4. Removal of the solvent in vacuum left a crude product, which was purified by silica gel column chromatography with n-heptane/EtOAc, followed by trituration with diethyl ether to give the title compound (46 mg, 13%) as a white solid. MS (ISP) 542.7 [(M+H)+]; mp 188° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183262B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-1c142560257447d182dfe002ff53ee7a |
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| Source note | uspto-grants-2012_05 |
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