Process for producing benzo[
A simple process for producing v-coelenterazine compounds has been desired. Described is a process for producing a v-coelenterazine compound represented by general formula (II) comprising (1) the step of reacting a compound of general formula (VIII) with a methyltriphenylphosphonium salt in the presence of a base to give a compound represented by general formula (IX), (2) the step of performing a ring-closing metathesis reaction on any one selected from the group consisting of the compound represented by general formula (IX) and a compound of general formula (X) which is the compound of general formula (IX) wherein the amino is protected with R 5 , and then deprotecting R 4 and, if any, R 5 to give a v-coelenteramine compound represented by general formula (XIV), and (3) the step of reacting the compound of general formula (XIV) with a compound represented by general formula (XV) to give the compound of general formula (II).
1. A process for producing a v-coelenteramine compound represented by formula (XIV):
(wherein R 1 is hydrogen; a halogen; an aryl which may optionally be substituted with at least one selected from the group consisting of a halogen, hydroxy, an alkyl having 1 to 6 carbon atoms, an alkoxy having 1 to 6 carbon atoms, an amino and a dialkylamino having 1 to 6 carbon atoms; an arylalkyl which may optionally be substituted with at least one selected from the group consisting of a halogen, hydroxy, an alkyl having 1 to 6 carbon atoms, an alkoxy having 1 to 6 carbon atoms, an amino and a dialkylamino having 1 to 6 carbon atoms; an arylalkenyl which may optionally be substituted with at least one selected from the group consisting of a halogen, hydroxy, an alkyl having 1 to 6 carbon atoms, an alkoxy having 1 to 6 carbon atoms, an amino and a dialkylamino having 1 to 6 carbon atoms; an alkyl which may optionally be substituted with an alicyclic group; an alkenyl which may optionally be substituted with an alicyclic group; an alicyclic group, a heterocyclic group; or an alkynyl which may optionally be substituted with an alicyclic group), which comprises:
(1) reacting a compound represented by formula (VIII):
(wherein R 1 is the same as defined above and R 4 is a protecting group selected from the group consisting of methyl, methoxymethyl, tetrahydropyranyl, benzyl, 4-methoxybenzyl, tert-butyldimethylsilyl, trimethylsilyl, triethylsilyl, phenyldimethylsilyl, tert-butyldiphenylsilyl and triisopropylsilyl) with a methyltriphenylphosphonium salt in the presence of a solvent and a base to give a compound represented by formula (IX):
(wherein R 1 and R 4 are the same as defined above), and,
(2) performing a ring-closing metathesis reaction on any one selected from the group consisting of the compound represented by formula (IX) and a compound represented by formula (X) which is prepared by protecting the amino in formula (IX) with R 5 :
(wherein R 1 and R 4 are the same as defined above and R 5 is a protecting group selected from the group consisting of acetyl, benzoyl, p-tosyl, tert-butoxycarbonyl and benzyloxycarbonyl) in the presence of a solvent and a catalyst, and then deprotecting R 4 and, if any, R 5 .
2. The process according to claim 1 , wherein at least one base selected from the group consisting of n-butyl lithium, potassium tert-butoxide, sodium methoxide, sodium ethoxide and lithium diisopropylamide is used as the base in step (1).
3. The process according to claim 1 , wherein at least one solvent selected from the group consisting of tetrahydrofuran, diethyl ether, cyclopropyl methyl ether, tert-butyl methyl ether, dioxane and toluene is used as the solvent in step (1).
4. The process according to claim 1 , wherein the reaction temperature and reaction time in step (1) are set at 0° C. to 40° C. for an hour to 4 hours.
5. The process according to claim 1 , wherein a second generation Hoveyda-Grubbs catalyst is used as the catalyst for the ring-closing metathesis reaction in step (2).
6. The process according to claim 1 , wherein at least one solvent selected from the group consisting of dichloroethane, dichloromethane, chloroform, trichloroethane, tetrachloroethane, benzene, toluene, xylene, monochlorobenzene, dichlorobenzene, hexane, heptane, octane, tetrahydrofuran, dioxane, diethyl ether, dibutyl ether, diisopropyl ether and dimethoxyethane is used as the solvent for the ring-closing metathesis reaction in step (2).
7. The process according to claim 1 , wherein the reaction temperature and reaction time of the ring-closing metathesis reaction in step (2) are set at 25° C. to 110° C. for an hour to 48 hours.