Process for the production of estetrol intermediates
The present invention relates to a process for the preparation of a compound of formula (I) said process comprising the steps of: a) reacting a compound of formula (II), with an acylating or a silylating agent to produce a compound of formula (III), wherein P 1 and P 2 are each independently a protecting group selected from R 2— Si—R 3 R 4 , or R 1 CO—, wherein R 1 is a group selected from C 1-6 alkyl or C 3-6 cycloalkyl, each group being optionally substituted by one or more substituents independently selected from fluoro or C 1-4 alkyl; R 2 , R 3 and R 4 are each independently a group selected from C 1-6 alkyl or phenyl, each group being optionally substituted by one or more substituents independently selected from fluoro or C 1-4 alkyl; b) reacting the compound of formula (III) in the presence of palladium acetate or a derivative thereof to produce compound of formula (IV); and c) reacting the compound of formula (IV) with a reducing agent to produce compound of formula (I).
1. A process for the preparation of a compound of formula (I)
said process comprising the steps of
a) reacting a compound of formula (II), with a silylating agent to produce a compound of formula (III), wherein P 1 is R 2— Si—R 3 R 4 , and P 2 is R 2— Si—R 3 R 4 , wherein R 2 , R 3 and R 4 are each independently a group selected from C 1-6 alkyl or phenyl, each group being optionally substituted by one or more substituents independently selected from fluoro or C 1-4 alkyl;
b) reacting the compound of formula (III) in the presence of palladium acetate or palladium chloride to produce a compound of formula (IV); and
c) reacting the compound of formula (IV) with a reducing agent to produce the compound of formula (I).
2. The process according to claim 1 , wherein the silylating agent is selected from the group comprising C 1-6 alkylsilylchloride, C 1-6 alkylsilyltriflate, phenylsilyl chloride, phenylsilyltriflate, C 1-6 alkylphenylsilylchloride, C 1-6 alkylphenylsilyltriflate, each group being optionally substituted by one or more substituents independently selected from fluoro or C 1-4 alkyl.
3. The process according to claim 1 , wherein step (b) is performed in the presence of a C 1-6 alkylene carbonate and an organotin compound.
4. The process according to claim 1 , wherein said palladium acetate or palladium chloride is present in stoichiometric amounts.
5. The process according to claim 1 , wherein said reaction is performed with palladium acetate or palladium chloride present in catalytic or sub-stoichiometric amounts.
6. The process according to claim 1 , wherein the reducing agent in step (c) is selected from the group of metal hydride compounds.
7. The process according to claim 6 , wherein the metal hydride compound is selected from the group consisting of NaBH 4 /CeCl 3 , LiAlH 4 , NaBH 4 , NaBH(OAc) 3 , and ZnBH 4 .
8. A process for the preparation of estetrol, said process comprising preparing a compound of formula (I) by a process,
said process comprising the steps of
a) reacting a compound of formula (II), with a silylating agent to produce a compound of formula (III), P 1 is R 2— Si—R 3 R 4 , and P 2 is R 2— Si—R 3 R 4 , wherein R 2 , R 3 and R 4 are each independently a group selected from C 1-6 alkyl or phenyl, each group being optionally substituted by one or more substituents independently selected from fluoro or C 1-4 alkyl;
b) reacting the compound of formula (III) in the presence of palladium acetate or palladium chloride to produce a compound of formula (IV); and
c) reacting the compound of formula (IV) with a reducing agent to produce the compound of formula (I), and further reacting the compound of formula (I) to produce the estetrol.
9. The process according to claim 5 , wherein said reaction is performed in an oxygen atmosphere.