تفاعل #11149

ord-63c40e69daaa436491abcccf68ef7925

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىprepared

الإجراء التجريبي

The reaction of 2-[2-(2-Chloro-6-methoxyphenyl)ethenyl]-5-methoxy-1H-indole (II; Ar=2-chloro-6-methoxyphenyl) (102) prepared as described in example 55 with 2-bromoethyl tetrahydro-2H-pyran-2-yl ether using the procedure described in example 38 followed by reaction of the crude product with 2N HCl in methanol gave 2-{2-[2-(2-Chloro-6-methoxyphenyl)ethenyl]-5-methoxy-1H-indol-1-yl}ethanol (III; Ar=2-chloro-6-methoxyphenyl, R10═CH2CH2OH) (109) in a 91% yield as a mixture of E/Z isomers, which was used without further purification.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07094798B1uspto-grants-2006_08