The present invention relates to a process for the preparation of a compound of formula (I) comprising the steps of a) reacting a compound of formula (II) with a silylating or an acylating agent to produce compound of formula (III), wherein P
1
is a protecting group selected from R
2
Si—R
3
R
4
or R
1
CO—, 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) halogenation or sulfinylation of the compound of formula (III) to produce a compound of formula (IV); wherein X is halo, or —O—SO—R
5
, and R
5
is a group selected from C
6-10
aryl or heteroaryl, each group being optionally substituted by one or more substituents independently selected from chloro or C
1-4
alkyl; c) dehalogenation or desulfinylation of the compound of formula (IV) to produce compound of formula (V); and d) reacting the compound of formula (V) with a reducing agent to produce compound of formula (I).
本发明涉及一种制备式(I)化合物的方法,包括以下步骤:a)将式(II)化合物与
硅化剂或酰化剂反应,生成式(III)化合物,其中P1是从R2Si—R3R4或R1CO—中选择的保护基,R1是从C1-6烷基或C3-6环烷基中选择的基团,每个基团都可以被一个或多个取代基独立地选择,所述取代基选择自
氟或C1-4烷基;R2、R3和R4各自独立地是从C1-6烷基或苯基中选择的基团,每个基团都可以被一个或多个取代基独立地选择,所述取代基选择自
氟或C1-4烷基;b)卤代或亚磺酰化式(III)化合物,生成式(IV)化合物;其中X是卤素或—O—SO—R5,R5是从C6-10芳基或杂环芳基中选择的基团,每个基团都可以被一个或多个取代基独立地选择,所述取代基选择自
氯或C1-4烷基;c)去卤代或去亚磺酰化式(IV)化合物,生成式(V)化合物;以及d)将式(V)化合物与还原剂反应,生成式(I)化合物。