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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175785Generated: November 1, 2026

Racemic benzyl 3-(hydroxymethyl)-3-methylpiperazine-1-carboxylate → benzyl 4-(2-hydroxy-2-((S)-3-methyl-1-oxoisochroman-6-yl)ethyl)-3-(hydroxymethyl)-3-methylpiperazine-1-carboxylate

https://huagongshe.com/reaction/2175785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantRacemic benzyl 3-(hydroxymethyl)-3-methylpiperazine-1-carboxylateHCID 68459606—
Reactant(3S)-3-Methyl-6-(oxiran-2-yl)-3,4-dihydro-1H-isochromen-1-oneHCID 86693038—
SolventEthanolHCID 702—
Productbenzyl 4-(2-hydroxy-2-((S)-3-methyl-1-oxoisochroman-6-yl)ethyl)-3-(hydroxymethyl)-3-methylpiperazine-1-carboxylateHCID 86727035—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of racemic benzyl 3-(hydroxymethyl)-3-methylpiperazine-1-carboxylate (1.0 g, 3.8 mmol) (prepared as described in US Patent Application Publication No. US2007/0088039A1, Example 10) in EtOH (13 mL) was added (3S)-3-methyl-6-(oxiran-2-yl)isochroman-1-one (773 mg, 3.80 mmol), the resulting mixture was heated at 80° C. for 16 h, the reaction mixture was concentrated to dryness and purified on silica gel to afford the title compound: LC/MS: m/e 469.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062070B2
Source datasetuspto-grants-2015_06
ORD IDord-86fc35c647054043b7b4e58fb8498924
Source noteuspto-grants-2015_06