تفاعل #93500

ord-e12560ad974f41aba543abacd5ee998d

معادلة التفاعل

Cl.O=C(CCC1CCNCC1)c1cc(C2CCCCC2)nc2ccccc12
1-(2-cyclohexyl-4-quinolyl)-3-(4-piperidyl)-1-propanone monohydrochloride
[BH4-].[Na+]
sodium borohydride
[Na+].[OH-]
sodium hydroxide
C[O-].[Na+]
sodium methylate
O=S(=O)([O-])[O-]
sulfate
OC(CCC1CCNCC1)c1cc(C2CCCCC2)nc2ccccc12
1-(2-cyclohexyl-4-quinolyl)-3-(4-piperidyl)-1-propanol
المردود 28.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

الإجراء التجريبي

The operation was as in Example 5, starting from 5.1 g of 1-(2-cyclohexyl-4-quinolyl)-3-(4-piperidyl)-1-propanone monohydrochloride, 1.3 ml of a 10N aqueous solution of sodium hydroxide (instead of sodium methylate) and 0.53 g of sodium borohydride in 100 ml of ethanol. 1.3 g of 1-(2-cyclohexyl-4-quinolyl)-3-(4-piperidyl)-1-propanol (racemic) were finally obtained in the form of the sulfate melting at 260° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04613607uspto-grants-1986_09