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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 579789생성일: 2026년 10월 26일

Dimethylformamide → 1-acetyl-N-(2-benzothiazolyl)-N-methyl-4-piperidinemethanamine

https://huagongshe.com/reaction/579789

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamineHCID 14048944—
용매WaterHCID 962—
생성물1-acetyl-N-(2-benzothiazolyl)-N-methyl-4-piperidinemethanamineHCID 2124158784%

반응 단계

A mixture of 8.7 part of 1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamine, 1.44 parts of a sodium hydride dispersion 60% and 270 parts of N,N-dimethylformamide was stirred for 1 hour at room temperature. 5.48 Parts of iodomethane were added dropwise slowly. Upon completion, stirring was continued overnight at room temperature. The reaction mixture was poured into water. The product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated in vacuo. The residue was purified by column chromatography (HPLC) over silica gel using a mixture of dichloromethane and methanol (98.75:1.25 by volume) as eluent. The second faction was collected and the eluent was evaporated, yielding 7.6 parts (84%) of 1-acetyl-N-(2-benzothiazolyl)-N-methyl-4-piperidinemethanamine as a residue (intermediate 52).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04749702
출처 데이터셋uspto-grants-1988_06
ORD IDord-0a615afa610c4cda9bbe82e6143ee075
출처 메모uspto-grants-1988_06