Hydrochloric Acid → HCID 11965693、化合物

A solution of 5-acetyl-2-amino-4-trifluoromethyl-benzoic acid methyl ester (10.2 g, 39.0 mmol) in THF (250 mL) was treated with (CCl3O)2CO (3.86 g, 12.9 mmol) and the mixture was stirred at r.t. for 15 min under nitrogen. To this solution was added Et3N (5.55 mL, 39.0 mmol) and the mixture was stirred for another 3 h at r.t. The mixture was then treated with CH3SO2NHNH2 (4.38 g, 39.0 mmol) and stirred for 1 h at r.t. Aqueous sodium hydroxide (1M, 78 mL, 78.0 mmol) was subsequently added and the solution was stirred for 18 h at r.t. The mixture was acidified with aqueous hydrochloric acid (4N) until pH=3-4, and then diluted with EtOAc. It was then washed once with water, and the organic phase was then dried over anhydrous sodium sulfate, filtered and concentrated until the product precipitated. The suspension was then cooled to 0° C., and then filtered. The white solid was dried in vacuo to give N-(6-acetyl-2,4-dioxo-7-trifluoromethyl-1,4-dihydro-2H-quinazolin-3-yl)-methanesulfonamide (12.1 g, 33.2 mmol, 85%), m.p. 258-265° C., ESI-MS: m/z 366 [M+H]+.

1. stirringthe mixture was stirred for another 3 h at r.t
2. stirringstirred for 1 h at r.t
3. stirringthe solution was stirred for 18 h at r.t
4. washIt was then washed once with water
5. dry with materialthe organic phase was then dried over anhydrous sodium sulfate
6. filtrationfiltered
7. concentrationconcentrated until the product
8. customprecipitated
9. temperatureThe suspension was then cooled to 0° C.
10. filtrationfiltered
11. customThe white solid was dried in vacuo

ORDレコード

ord-5679f0f80fc8463c8e68766625ac6baf

出典データセット

uspto-grants-2010_02

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07655666B2