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HRID 46856作成日:2026年10月26日

Triethylamine → 4-chloro-1,3-dihydro-3-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate

https://huagongshe.com/reaction/46856

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4-chloro-1,3-dihydro-3-(3-hydroxypropyl)-2H-benzimidazol-2-oneHCID 20385560—
溶媒DichloromethaneHCID 6344—
生成物4-chloro-1,3-dihydro-3-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonateHCID 8673535875%

反応手順

To a stirred mixture of 9 parts of 4-chloro-1,3-dihydro-3-(3-hydroxypropyl)-2H-benzimidazol-2-one, 7 parts of N,N-diethylethanamine and 130 parts of dichloromethane are added dropwise 12 parts of methanesulfonyl chloride (exothermic reaction: temperature rises to reflux). Upon completion, stirring is continued for 1 hour at reflux temperature. The reaction mixture is cooled and poured onto water. The organic phase is separated, washed with acidified water, dried, filtered and evaporated. The residue is crystallized from 4-methyl-2-pentanone, yielding 9 parts (75%) of 4-chloro-1,3-dihydro-3-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04175129
出典データセットuspto-grants-1979_11
ORD IDord-d502e62f63db497e9620781e7b93099a
出典メモuspto-grants-1979_11