HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → n-(2,4-Dioxo-6-pyrazin-2-yl-7-trifluoromethyl-1,4-dihydro-2h-quinazolin-3-yl)-methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Chlorophenyl chloroformate | HCID 139059 | — |
| Reactant | Methanesulfonohydrazide | HCID 269268 | — |
| Reactant | 2-Amino-5-pyrazin-2-yl-4-trifluoromethyl-benzoic acid methyl ester | HCID 11965782 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | n-(2,4-Dioxo-6-pyrazin-2-yl-7-trifluoromethyl-1,4-dihydro-2h-quinazolin-3-yl)-methanesulfonamide | HCID 11965783 | 76.2% |
Reaction Steps
A solution of 2-amino-5-pyrazin-2-yl-4-trifluoromethyl-benzoic acid methyl ester (235 mg, 0.79 mmol) and 4-chlorophenyl chloroformate (133 μL, 0.95 mmol) in dioxane (8 mL) was stirred at 80° C. for 105 min. After cooling to r.t., CH3SO2NHNH2 (130.6 mg, 1.19 mmol) and i-Pr2NEt (276 μL, 1.58 mmol) were added. The mixture was heated to 80° C. for 45 min, cooled to r.t., and the solvent was removed in vacuo. The residue was purified by flash chromatography (50 g silica gel, DCM→MeOH in DCM (2% to 5%)) to provide the title compound (241.5 mg, 76%) as a white powder. API-ES: m/z 402 [M+H]+, rt 2.69 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513268B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-0275d18eee8a42a2b7fe7ba90b27cc45 |
| Source note | uspto-grants-2013_08 |