반응 #339058

ord-15abb22acc9d4902b84699afde4fba8b

반응 방정식

CN1Cc2c(Cl)cc(Cl)cc2[C@H](c2ccccc2N)C1
(R)-2-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydro-isoquinolin-4-yl)phenylamine
O=C(Cl)OCCCl
2-chloroethyl chloroformate
CN1Cc2c(Cl)cc(Cl)cc2[C@H](c2ccccc2N2CCOC2=O)C1
desired product
수율 108.6%
CN1Cc2c(Cl)cc(Cl)cc2[C@H](c2ccccc2N2CCOC2=O)C1
3-[2-((R)-6,8-Dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenyl]-oxazolidin-2-one
수율 108.6%

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

Analogously to example 45a), (R)-2-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydro-isoquinolin-4-yl)phenylamine (300 mg, enantiomer B, preparation as described in WO2004085404) was reacted with 2-chloroethyl chloroformate (140 mg). 400 mg of the desired product were obtained.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07868003B2uspto-grants-2011_01