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HRID 971739作成日:2026年10月25日

Triethylamine → 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate

https://huagongshe.com/reaction/971739

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-oneHCID 3017358—
溶媒DichloromethaneHCID 6344—
生成物5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonateHCID 8673535953%

反応手順

To a stirred and cooled (ice-water bath) mixture of 14.1 parts of 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one, 8 parts of N,N-diethylethanamine and 195 parts of dichloromethane are added dropwise 7.8 parts of methanesulfonyl chloride. Upon completion, stirring is continued first for 15 minutes while still cooling an further for 1 hour at reflux temperature. The dichloromethane is evaporated and the residue is dissolved in 4-methyl-2-pentanone and water while heating. The layers are separated and the organic phase is stirred with 100 parts of water, while cooling in an ice-bath. The precipitated product is filtered off and dried, yielding 10 parts (53%) of 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate; mp. 140° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04160836
出典データセットuspto-grants-1979_07
ORD IDord-3147bbec8b5041ac8aeadd298b5c2740
出典メモuspto-grants-1979_07