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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231075Generated: October 31, 2026

1-Methylpiperazine → HCID 14579227, compound

https://huagongshe.com/reaction/231075

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 14579226HCID 14579226—
SolventBenzeneHCID 241—
ProductHCID 14579227HCID 1457922755.1%

Reaction Steps

970 mg (3.1 m moles) of 4-bromo-2-phenyl-2,3,4,5-tetrahydro-1-benzoxepin-5-one (compound R14 of Reference Example 14) was dissolved in 100 ml of benzene, 3.1 g (10 equivalent amount) of N-methylpiperazine was added to the solution, and the whole was heated to reflux for 7 hours. After distilling off the solvent, water was added to the residue, and the mixture was extracted with methylene chloride. The organic phase was washed with water and dried with anhydrous magnesium sulfate. After filtrating off the magnesium sulfate, the filtrate was concentrated to obtain a residue, which was then applied to a silica gel column, and eluted with a mixture of methylene chloride/methanol (90:10) to obtain diastereomers R15a (700 mg; yield 55.1%) and R15b (220 mg; yield 17.3%) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04845094
Source datasetuspto-grants-1989_07
ORD IDord-190e4b55d8874a88a2e53cb4806f63ac
Source noteuspto-grants-1989_07