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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789495Generated: October 25, 2026

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

https://huagongshe.com/reaction/1789495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant1-acetyl-N-(2-benzothiazolyl)-4-piperidinemethanamineHCID 14048944—
SolventWaterHCID 962—
Product1-acetyl-N-(2-benzothiazolyl)-N-methyl-4-piperidinemethanamineHCID 2124158784%

Reaction Steps

A mixture of 8.7 parts 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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04689330
Source datasetuspto-grants-1987_08
ORD IDord-8ac978557b4942dd8db7d2fbfc8ff579
Source noteuspto-grants-1987_08