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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723436Generated: November 3, 2026

Dimethylformamide → HCID 14575317, compound

https://huagongshe.com/reaction/1723436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 11961759HCID 11961759—
ReactantHCID 14575306HCID 14575306—
ProductHCID 14575317HCID 1457531749%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4.4 parts of 1-chloro-3-(4-chlorobutoxy)benzene, 3.7 parts of N-methyl-N-(4-piperidinyl)-2-benzothiazolamine, 2.1 parts of sodium carbonate and 90 parts of N,N-dimethylformamide was stirred for 24 hours at 60° C. The reaction mixture was cooled and poured onto water. The product was extracted with methylbenzene. The extract was washed with water, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (97:3 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was converted into the (Z)-2-butenedioate salt in 2-propanone. The salt was filtered off and dried, yielding 4 parts (49%) of N-[1-[4-(3-chlorophenoxy)butyl]-4-piperidinyl]-N-methyl-2-benzothiazolamine (Z)-2-butenedioate (1:1); mp. 138.6° C. (1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04861785
Source datasetuspto-grants-1989_08
ORD IDord-ad8b3ebfc1814be3aa083061ab735b37
Source noteuspto-grants-1989_08