WO2007126122A1

WO2007126122A1 - Dihydropyrazolopyrimidinone derivatives

Info

Publication number: WO2007126122A1
Application number: PCT/JP2007/059408
Authority: WO
Inventors: Toshihiro Sakamoto; Satoshi Sunami; Fuyuki Yamamoto; Kenji Niiyama; Makoto Bamba; Keiji Takahashi; Hidetomo Furuyama; Takeshi Sagara; Sachie Otsuki; Toshihide Nishibata; Takashi Yoshizumi; Hiroshi Hirai
Original assignee: Banyu Pharmaceutical Co., Ltd.
Priority date: 2006-04-27
Filing date: 2007-04-25
Publication date: 2007-11-08
Also published as: SI2017278T1; EP2017278A1; IL194367A; KR101409161B1; IL194367A0; US20140303178A1; HUE032987T2; SV2009003060A; EP2016080A4; DOP2007000084A; CN101432284A; HN2008001532A; US20070254892A1; MY145408A; JP2010132689A; PL2017278T3; ZA200807748B; US7834019B2; ATE475662T1; HK1132498A1

Abstract

The invention relates to compounds of a general formula (I): wherein A1 is selected from the following formula (aa1); R1 is a lower alkenyl group or a lower alkynyl group; R2 is a phenyl, pyridyl or thienyl group; R5 and R6 are a hydrogen atom, a lower alkyl group or a hydroxy-lower alkyl group, etc. The compounds of the invention have excellent Weel kinase-inhibitory effect and are therefore useful in the field of medicines, especially treatment of various cancers.

Description

DESCRIPTION

DIHYDROPYRAZOLOPYRIMIDINONE DERIVATIVES

Technical Field

The present invention is useful in the field of medicine. More precisely, the dihydropyrazolopyrimidinone derivatives of the invention are useful in the field of treatment of various cancers as a kinase inhibitor, especially as a Weel kinase inhibitor.

Background Art

Cells have a checkpoint mechanism of such that, when the DNA therein is damaged, then the cells temporarily stop the cell cycle and repair the damaged DNA (Cell Proliferation, Vol. 33, pp. 261-274). In about a half of human cancers, a cancer-suppressor gene, p53 is mutated or depleted and the cells thereby have lost the Gl checkpoint function thereof. However, such cancer cells still keep the G2 checkpoint function remaining therein, which is considered to be one factor of lowering the sensitivity of the cells to DNA-active anticancer agents and to radiations.

A Weel kinase is a tyrosine kinase that participates in the G2 checkpoint of a cell cycle. Weel phosphorylates Cdc2(Cdkl) tyrosine 15 that participates in the progress to the M stage from the G2 stage in a cell cycle, thereby inactivating Cdc2 and temporarily stopping the cell cycle at the G2 stage (Tfie EMBO Journal, Vol. 12, pp. 75-85). Accordingly, in cancer cells having lost the p53 function therein, it is considered that the G2 checkpoint function by Weel is important for repairing the damaged DNA so as to evade the cell death. Heretofore, it has been reported that the Weel expression reduction by RNA interference or the Weel inhibition by compounds may increase the sensitivity of cancer cells to adriamycin, X ray and gamma ray (Cancer Biology & Therapy, Vol. 3, pp. 305-313; Cancer Research, Vol. 61, pp. 8211-8217). From the above, it is considered that a Weel inhibitor may inhibit the G2 checkpoint function of p53-depleted cancer cells, thereby enhancing the sensitivity of the cells to DNA-active anticancer agents and to radiations.

As a low-molecular Weel kinase inhibitor, for example, known are compounds described in US Application 2005/0250836, WO2003/091255, Cancer Research, Vol. 61, pp. 8211-8217, orBioorg &Med. Chem. Lett, Vol. 15, pp. 1931-1935. However, the compounds described in these references quite differ from the compounds of the invention in point of their structures.

On the other hand, WO2004/056786, WO2005/021532 or WO2006/091737 disclose various compounds such as dihydropyrazolopyridines that are relatively similar to the compounds of the invention in point of their skeletons. However, these references do neither concretely disclose nor suggest any Weel kinase-inhibitory effect of those compounds as well as the compounds of the invention.

Disclosure of Invention

An object of the invention is to provide a novel anticancer agent having a kinase- inhibitory effect, especially a Weel kinase-inhibitory effect.

As a result of assiduous studies, the present inventors have found that compounds of the following general formula (I) have an excellent kinase-inhibitory effect, especially an excellent Weel kinase-inhibitory effect, and have completed the present invention: R¹ _R2

H wherein,

Al is selected from the following formula (aal):

RIC is a hydrogen atom, a lower alkenyl group or a group of -Q3-A3(Rld)Rle;

A3 is a nitrogen atom, or is a methine or l-vinyl-2-ylidene group optionally substituted by a hydroxyl group, a lower alkyl group or a hydroxy-lower alkyl group;

Q3 is a single bond or a lower alkylene group, wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom, a sulfur atom, a carbonyl group, a sulfinyl group or a sulfonyl group, and/or substituted by a halogen atom, a cyano group, a hydroxyl group or a lower alkyl group;

Rid and Rl ^e are independently a hydrogen atom, a halogen atom, a cyano group, a hydroxyl group, a lower alkyl group or a hydroxy-lower alkyl group, or together form a lower alkylene group wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom, a sulfur atom, a sulfinyl group, a sulfonyl group, a carbonyl group, a vinylene group or a group of -N(Rlf)-, and/or substituted by a hydroxyl group or a lower alkyl group;

Rlf is a hydrogen atom, a lower alkyl group, a halo-lower alkyl group, a lower alkenyl group or a lower alkanoyl group;

Rl is a lower alkenyl group or a lower alkynyl group; R2 is a phenyl, pyridyl or thienyl group, which may have a group of -Q4- A4(Rlg)Rlh_;

A4 is a nitrogen atom, or is a methine group optionally substituted by a halogen atom, a hydroxyl group, a lower alkyl group or a hydroxy-lower alkyl group;

Q4 is a single bond or a lower alkylene group, wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom or a carbonyl group, and/or substituted by a lower alkyl group;

Rig and Rlh are independently a hydrogen atom, a halogen atom, a cyano group, a hydroxyl group, a lower alkyl group, a lower alkoxy-lower alkyl group, a lower alkanoyl group, a lower alkoxycarbonyl group or a lower alkylsulfonyl group, or together form a lower alkylene group, wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom, a sulfur atom, a sulfinyl group, a sulfonyl group, a carbonyl group or a group of -N(RU)-, and/or substituted by a halogen atom or a lower alkyl group;

Rli is a hydrogen atom, a lower alkyl group or a halo-lower alkyl group;

R5 and R6 are independently a hydrogen atom, a lower alkyl group or a hydroxy- lower alkyl group.

The compounds (I) of the invention have a kinase-inhibitory effect, especially a Weel kinase-inhibitory effect, and are therefore useful as remedies for various cancers such as brain cancer, cervicocerebral cancer, esophageal cancer, thyroid cancer, small cell cancer, non- small cell cancer, breast cancer, lung cancer, stomach cancer, gallbladder/bile duct cancer, liver cancer, pancreatic cancer, colon cancer, rectal cancer, ovarian cancer, choriocarcinoma, uterus body cancer, uterocervical cancer, renal pelvis/ureter cancer, bladder cancer, prostate cancer, penis cancer, testicles cancer, fetal cancer, Wilms' cancer, skin cancer, malignant melanoma, neuroblastoma, osteosarcoma, Ewing's tumor, soft part sarcoma, acute leukemia, chronic lymphatic leukemia, chronic myelocytic leukemia, Hodgkin's lymphoma.

In particular, the compounds (I) of the invention are useful as remedies, for example, for breast cancer, lung cancer, pancreatic cancer, colon cancer, ovarian cancer, acute leukemia, chronic lymphatic leukemia, chronic myelocytic leukemia, Hodgkin's lymphoma.

The invention relates to the compounds of formula (I) and their salts, as well as to their production methods and their use.

The meanings of the terms used in this description are described below, and the invention is described in more detail hereinunder.

"Halogen atom" means a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.

"Lower alkyl group" means a linear or branched alkyl group having from 1 to 6 carbon atoms, including, for example, a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, an isopentyl group, a hexyl group, an isohexyl group.

"Halo-lower alkyl group" means the above-mentioned lower alkyl group in which any substitutable position is substituted by one or two or more, preferably from 1 to 3, the same or different, above-mentioned halogen atoms, including, for example, a fluoromethyl group, a difluoromethyl group, a trifluoromethyl group, a 2-fluoroethyl group, a 1,2-difluoroethyl group, a chloromethyl group, a 2-chloroethyl group, a 1,2-dichloroethyl group, a bromomethyl group, an iodomethyl group.

"Hydroxy-lower alkyl group" means the above-mentioned lower alkyl group in which any substitutable position is substituted by one or two or more, preferably 1 or 2 hydroxyl groups, including, for example, a hydroxymethyl group, a 2-hydroxyethyl group, a 1-hydroxy-l- methylethyl group, a 1,2-dihydroxyethyl group, a 3-hydroxypropyl group.

"Lower alkoxy group" means a linear or branched alkoxy group having from 1 to 6 carbon atoms, including, for example, a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, a butoxy group, a sec-butoxy group, an isobutoxy group, a tert-butoxy group, a pentyloxy group, an isopentyloxy group, a hexyloxy group, an isohexyloxy group.

"Lower alkanoyl group" means an alkanoyl group having the above-mentioned lower alkyl group, or that is, an alkanoyl group having from 2 to 7 carbon atoms, including, for example, an acetyl group, a pfopionyl group, a butyryl group, an isobutyryl group, a valeryl group, an isovaleryl group, a pivaloyl group.

"Lower alkylene group" means a linear or branched alkylene group having from 1 to 6 carbon atoms, including, for example, a methylene group, an ethylene group, a trimethylene group, a tetramethylene group, a pentamethylene group, a hexamethylene group.

"Lower alkenyl group" means a linear or branched alkenyl group having from 2 to 6 carbon atoms, including, for example, a vinyl group, a 1-propenyl group, an allyl group, an isopropenyl group, a 3-butenyl group, a 2-butenyl group, a 1-butenyl group, a l-methyl-2- propenyl group, a 1 -methyl- 1-propenyl group, a 1-ethyl-l-ethenyl group, a 2-methyl-2-propenyl group, a 2-methyl- 1-propenyl group, a 3-methyl-2-butenyl group, a 4-pentenyl group.

"Lower alkynyl group" means a linear or branched alkynyl group having from 2 to 6 carbon atoms, including, for example, an ethynyl group, a 1-propynyl group, a 2-propynyl group, a 3-butynyl group, a 2-butynyl group, a 1-butynyl group, a l-methyl-2-propynyl group, a l-ethyl-2-propynyl group, a l-methyl-2-butynyl group, a 4-pentynyl group.

"Lower alkoxy-lower alkyl group" means the above-mentioned lower alkyl group in which any substitutable position is substituted by one or two or more, preferably 1 or 2, the same or different, above-mentioned lower alkoxy groups, including, for example, a methoxymethyl group, an ethoxymethyl group, a 2-methoxyethyl group, a 2-ethoxyethyl group, a 1 -methoxy- 1-methylethyl group, a 1,2-dimethoxyethyl group, a 3-methoxypropyl group. "Lower alkoxycarbonyl group" means an alkoxycarbonyl group having the above- mentioned lower alkoxy group, or that is, an alkoxycarbonyl group having from 2 to 7 carbon atoms, including, for example, a methoxycarbonyl group, an ethoxycarbonyl group, a propoxycarbonyl group, an isopropoxycarbonyl group, a butoxycarbonyl group, an isobutoxycarbonyl group, a tert-butoxycarbonyl group, a pentyloxycarbonyl group.

"Lower alkylsulfonyl group" means a linear or branched alkylsulfonyl group having from 1 to 6 carbon atoms, including, for example, a methylsulfonyl group, an ethylsulfonyl group, a propylsulfonyl group, an isopropylsulfonyl group, a butylsulfonyl group, a sec-butylsulfonyl group, an isobutylsulfonyl group, a tert-butylsulfonyl group, a pentylsulfonyl group, an isopentylsulfonyl group, a hexylsulfonyl group, an isohexylsulfonyl group.

"Salts" of the compounds of the invention mean ordinary, pharmaceutically- acceptable salts. For example, when the compounds have a carboxyl group, a hydroxyl group, or an acidic heterocyclic group such as a tetrazolyl group, then they may form base-addition salts at the carboxyl group, the hydroxyl group or the acidic heterocyclic group; or when the compounds have an amino group or a basic heterocyclic group, then they may form acid-addition salts at the amino group or the basic heterocyclic group.

The base-addition salts include, for example, alkali metal salts such as sodium salts, potassium salts; alkaline earth metal salts such as calcium salts, magnesium salts; ammonium salts; and organic amine salts such as trimethylamine salts, triethylamine salts, dicyclohexylamine salts, ethanolamine salts, diethanolamine salts, triethanolamine salts, procaine salts, N,N'-dibenzylethylenediamine salts.

The acid-addition salts include, for example, inorganic acid salts such as hydrochlorides, sulfates, nitrates, phosphates, perchlorates; organic acid salts such as maleates, fumarates, tartrates, citrates, ascorbates, trifluoroacetates; and sulfonates such as methanesulfonates, isethionates, benzenesulfonates, p-toluenesulfonates.

"Esters" of the compounds of the invention means ordinary pharmaceutically- acceptable esters at the carboxyl group, if any, of the compounds. They include, for example, esters with a lower alkyl group such as a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, an isopentyl group, a neopentyl group, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group; esters with an aralkyl group such as a benzyl group, a phenethyl group; esters with a lower alkenyl group such as an allyl group, a 2-butenyl group; esters with a lower alkoxy-lower alkyl group such as a methoxymethyl group, a 2-methoxyethyl group, a 2-ethoxyethyl group; esters with a lower alkanoyloxy-lower alkyl group such as an acetoxymethyl group, a pivaloyloxymethyl group, a 1-pivaloyloxy ethyl group; esters with a lower alkoxycarbonyl-lower alkyl group such as a methoxycarbonylmethyl group, an isopropoxycarbonylmethyl group; esters with a carboxy- lower alkyl group such as a carboxymethyl group; esters with a lower alkoxycarbonyloxy-lower alkyl group such as a l-(ethoxycarbonyloxy)ethyl group, a l-(cyclohexyloxycarbonyloxy)ethyl group; esters with a carbamoyloxy-lower alkyl group such as a carbamoyloxymethyl group; esters with a phthalidyl group; esters with a (5-substituted-2-oxo-l,3-dioxol-4-yl)methyl group such as a (5-methyl-2-oxo-l,3-dioxol-4-yl)methyl group.

For illustrating the compounds of the invention more concretely, preferred examples of the symbols used in formula (I) and others are described below in more detail.

Rl is a lower alkenyl group or a lower alkynyl group.

The "lower alkenyl group" for Rl is, for example, preferably an allyl group, a 2- methyl-2-propenyl group, a 3-methyl-2-butenyl group, especially preferably an allyl group.

The "lower alkynyl group" for Rl is, for example, preferably a 2-propynyl group.

Preferred embodiments of Rl are, for example, a lower alkenyl group optionally substituted by a halogen atom, more concretely, an allyl group, a 2-methyl-2-propenyl group, a 3- methyl-2-butenyl group; more preferably an allyl group.

Another preferred embodiments of Rl are, for example, a lower alkynyl group optionally substituted by a halogen atom, more concretely, a 2-propynyl group.

Especially a lower alkenyl group such as an allyl group etc.is preferred for Rl.

Rl is, for example, preferably an allyl group, a 2-methyl-2-propenyl group, a 3- methyl-2-butenyl group, a 2-propynyl group, more preferably an allyl group.

R2 is a phenyl, pyridyl or thienyl group, which may have a group of -Q4- A4(Rlg)Rlh

The "phenyl, pyridyl or thienyl group, which may have a group of -Q4-

A4(Rlg)Rlh^M for R2 means the above-mentioned unsubstituted phenyl, pyridyl or thienyl group, or the above-mentioned phenyl, pyridyl or thienyl group substituted by the group of -Q4- A4(Rlg)Rlh. The group may have the same or different, one or two or more, preferably 1 or 2 groups of -Q4-A4(Rlg)Rlh at any substitutable position therein.

In the group of -Q4-A4(Rlg)Rlh for the substituent, A4 is a nitrogen atom, or is a methine group optionally substituted by a halogen atom, a hydroxyl group, a lower alkyl group or a hydroxy-lower alkyl group; Q4 is a single bond or a lower alkylene group, wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom or a carbonyl group, and/or substituted by a lower alkyl group; Rig and Rlh are independently a hydrogen atom, a halogen atom, a cyano group, a hydroxyl group, a lower alkyl group, a lower alkoxy-lower alkyl group, a lower alkanoyl group, a lower alkoxycarbonyl group or a lower alkylsulfonyl group, or together form a lower alkylene group, wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom, a sulfur atom, a sulfinyl group, a sulfonyl group, a carbonyl group or a group of -N(RU)-, and/or substituted by a halogen atom or a lower alkyl group. The "methine group optionally substituted by a halogen atom, a hydroxyl group, a lower alkyl group or a hydroxy-lower alkyl group" for A4 means an unsubstituted methine group, or a methine group having a substituent selected from a group consisting of a halogen atom, a hydroxyl group, a lower alkyl group and a hydroxy-lower alkyl group.

One or two or more methylene groups constituting the lower alkylene group for Q4 may be independently replaced by an oxygen atom or a carbonyl group, and/or substituted by a lower alkyl group.

The lower alkylene group that Rig and Rlh together form is, for example, preferably an ethylene group, a trimethylene group, a tetramethylene group, a pentamethylene group. When "A4" to which they bond is a nitrogen atom, then they form along with the nitrogen atom, a 1-aziridinyl group, a 1-azetidinyl group, a 1-pyrrolidinyl group, a piperidino group; when "A4^M is a methine group, they form along with the methine group, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group. Above all, more preferred are a 1- pyrrolidinyl group, a piperidino group, a cyclobutyl group, a cyclohexyl group.

One or two or more methylene groups constituting the above-mentioned lower alkylene group may be independently replaced by an oxygen atom, a sulfur atom, a sulfinyl group or a sulfonyl group, a carbonyl group or a group of -N(RU)-, and/or substituted by a halogen atom or a lower alkyl group. Examples of the replaced or substituted groups are preferably selected from the following formula (bb3'):

Rli in the group of -N(RU)- is a hydrogen atom, a lower alkyl group or a halo- lower alkyl group.

The lower alkyl group for Rli is, for example, preferably a methyl group, an ethyl group.

The halo-lower alkyl group for Rli is, for example, preferably a fluoromethyl group, a difluoromethyl group.

Preferred embodiments of the group of -Q4-A4(Rlg)Rlh are, for example, as follows:

(i) A4 is a nitrogen atom, Q4 is a single bond or a methylene group optionally substituted by a lower alkyl group, and Rig and Rlh are independently a hydrogen atom, a lower alkyl group, a lower alkanoyl group, a lower alkoxycarbonyl group or a lower alkylsulfonyl group;

(ii) A4 is a nitrogen atom or is a methine group optionally substituted by a halogen atom, a hydroxyl group, a lower alkyl group or a hydroxy-lower alkyl group, Q4 is a carbonyl group, and Rig and Rlh are independently a hydrogen atom or a lower alkyl group; (iii) A4 is a methine group optionally substituted by a halogen atom, a hydroxyl group, a lower alkyl group or a hydroxy-lower alkyl group, Q4 is a single bond or a methylene group optionally replaced by an oxygen atom, and Rig and Rlh are independently a hydrogen atom, a halogen atom, a hydroxyl group, a lower alkyl group or a lower alkoxycarbonyl group;

(iv) A4 is a methine group optionally substituted by a halogen atom, a hydroxyl group, a lower alkyl group or a hydroxy-lower alkyl group, Q4 is a single bond, and Rig and Rlh together form a lower alkylene group, in which one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom or a group of -N(RIi)-; _Or

(v) A4 is a nitrogen atom, Q4 is a single bond, and Rig and Rlh together form a lower alkylene group, in which one or two or more methylene groups constituting the lower alkylene group may be independently replaced by a carbonyl group or a group of -N(RU)-; more preferably above (iii).

More concretely, the group of -Q4-A4(Rlg)Rlh is, for example, preferably an amino group, a dimethylaminomethyl group, a methylsulfonylamino group, an N-methyl-N- methylsulfonylaminomethyl group, a carbamoyl group, a dimethylcarbamoyl group, a methyl group, a 1-fluoro-l-methylethyl group, a hydroxymethyl group, a 1 -hydroxy- 1-methylethyl group, a 2-hydroxy-l,l-dimethylethyl group, a 2-hydroxy-2-methylpropyl group, a 2-hydroxy-l,l- dimethylpropyl group, a methoxy group, a 2-hydroxyethoxy group, a 1-hydroxycyclobutyl group, a 2-oxo-l-pyrrolidinyl group, or a 3-methyl-2-oxoimidazolidin-l-yl group, even more preferably a 1 -hydroxy- 1-methylethyl group etc..

Preferred embodiments of R2 are, for example, a phenyl or pyridyl, more preferably pyridyl group having a group of -Q4-A4(Rlg)Rlh.

Concretely, therefore, the phenyl, pyridyl or thienyl group which may have the group of -Q4-A4(Rlg)Rlh for R2 is, for example, preferably a phenyl group, a 3- dimethylaminomethylphenyl group, a 3-dimethylcarbamoylphenyl group, a 3-(l-hydroxy-l- methylethyl)phenyl group, a 3-thienyl group, a 2-pyridyl group, a 6-amino-2-pyridyl group, a 6- (N-methyl-N-methylsulfonylaminomethyl)-2-pyridyl group, a 6-methyl-2-pyridyl group, a 6-(l- hydroxy-l-methylethyl)-2-pyridyl group, a 6-(2-hydroxy-l,l-dimethylethyl)-2-pyridyl group, a 6- (2-hydroxy-2-methylpropyl)-2-pyridyl group, a 6-(2-hydroxy-l,l-dimethylpropyl)-2-pyridyl group, a 6-(2-hydroxyethoxy)-2-pyridyl group, a 6-(l-hydroxycyclobutyl)-2-pyridyl group, a 6- (2-oxo-l-pyrrolidinyl)-2-pyridyl group, or a 6-(3-methyl-2-oxoimidazolidin-l-yl)-2-pyridyl group, more preferably a 6-(l-hydroxy-l-methylethyl)-2-pyridyl group etc.

Preferred embodiments of Rl and R2 in formula (I) are, for example, Rl is a lower alkenyl or lower alkynyl, more preferably lower alkenyl group, and R2 is a phenyl or pyridyl, more preferably pyridyl group having a group of -Q4-A4(Rlg)Rlh.

Al in formula (I) is selected from the following formula (aal):

RIC in the group of -N(RIc)- is a hydrogen atom, a lower alkenyl group or a group of -Q3-A3(Rld)Rle.

The lower alkenyl group for Rl° is, for example, preferably a vinyl group, an allyl group.

In the group of -Q3-A3(Rld)Rle for RIc₅ A3 is a nitrogen atom, or is a methine or l-vinyl-2-ylidene group optionally substituted by a hydroxyl group, a lower alkyl group or a hydroxy-lower alkyl group; Q3 is a single bond or a lower alkylene group, wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom, a sulfur atom, a carbonyl group, a sulfinyl group or a sulfonyl group, and/or substituted by a halogen atom, a cyano group, a hydroxyl group or a lower alkyl group; Rid and Rl^e are independently a hydrogen atom, a halogen atom, a cyano group, a hydroxyl group, a lower alkyl group or a hydroxy-lower alkyl group, or together form a lower alkylene group wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom, a sulfur atom, a sulfinyl group, a sulfonyl group, a carbonyl group, a vinylene group or a group of -N(Rlf)-, and/or substituted by a hydroxyl group or a lower alkyl group.

The "methine or l-vinyl-2-ylidene group optionally substituted by a hydroxyl group, a lower alkyl group or a hydroxy-lower alkyl group" for A3 means an unsubstituted methine or l-vinyl-2-ylidene group, or a methine or l-vinyl-2-ylidene group having a substituent selected from a group consisting of a hydroxyl group, a lower alkyl group and a hydroxy-lower alkyl group.

The substituent is preferably a hydroxyl group, a lower alkyl group such as a methyl group and an ethyl group.

The lower alkylene group for Q3 is, for example, preferably a methylene group, an ethylene group, a trimethylene group.

One or two or more methylene groups constituting the lower alkylene group for Q3 may be independently replaced by an oxygen atom, a sulfur atom, a carbonyl group, a sulfinyl group or a sulfonyl group, and/or substituted by a halogen atom, a cyano group, a hydroxyl group or a lower alkyl group.

The halogen atom for Rid or Rle is, for example, preferably a fluorine atom, a chlorine atom.

The lower alkyl for Rid or Rl^e is, for example, preferably a methyl group, an ethyl group. The hydroxy-lower alkyl group for Rid or Rle is, for example, preferably a hydroxymethyl group, a 2-hydroxyethyl group.

The lower alkylene group which for Rid and Rl^e together form is, for example, preferably an ethylene group, a trimethylene group, a tetramethylene group. When "A3" to which they bond is a nitrogen atom, then they form along with the nitrogen atom, a 1-aziridinyl group, a 1-azetidinyl group, a 1-pyrrolidinyl group; when "A3" is a methine group, they form along with the methine group, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group; when "A3" is a l-vinyl-2-ylidene group, then they form along with the l-vinyl-2-ylidene group, a 1-cyclobutenyl group, a 1-cyclopentenyl group, a 1-cyclohexenyl group. Above all, more preferred are a cyclopropyl group, a cyclobutyl group, a cyclopentyl group.

One or two or more methylene groups constituting the above-mentioned lower alkylene group may be independently replaced by an oxygen atom, a sulfur atom, a sulfinyl group or a sulfonyl group, a carbonyl group, a vinylene group or a group of -N(Rlf)-, and/or substituted by a hydroxyl group or a lower alkyl group.

Rlf in the group of -N(RIf)- is a hydrogen atom, a lower alkyl group, a halo- lower alkyl group, a lower alkenyl group or a lower alkanoyl group.

Preferred embodiments of the group of -Q_3-A3(Rld)Rle are, for example, as follows:

(i) A3 is a methine group optionally substituted by a hydroxyl group or a lower alkyl group, Q3 is a single bond, and Rid and Rle are independently a hydrogen atom or a lower alkyl group; or

(ii) A3 is a methine group optionally substituted by a hydroxyl group or a lower alkyl group, Q3 is a lower alkylene group wherein one or two methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom, a carbonyl group or a sulfonyl group, and/or substituted by a hydroxyl group, and Rid and Rle are independently a hydrogen atom, a halogen atom, a cyano group or a lower alkyl group; more preferably above (i).

More concretely, the group of -Q3-A3(Rld)Rle i_Sj for example, preferably a methyl group, an ethyl group, a propyl group, an isopropyl group, a tert-butyl group, a hydroxymethyl group, a 1 -hydroxy- 1-methylethyl group, a 2-hydroxyethyl group, a 2- methoxyethyl group, a 2-ethoxyethyl group, a 2-hydroxy-2-methylpropyl group, a 3-fluoro-2- hydroxypropyl group, an acetyl group, a propionyl group, a 2-methoxyacetyl group, a tert- butoxycarbonyl group, a methylsulfonyl group, a 2-(methylsulfonyl)ethyl group; more preferably a methyl group, an ethyl group, a tert-butyl group, a 2-hydroxyethyl group, a 2-methoxyethyl group, an acetyl group; more preferably a methyl group..

RIC is preferably a hydrogen atom or a group of -0,3-AS(RId)RIe_^ more preferably a group of -Q3-A3(Rld)Rle. .

Preferred embodiments of Al are, for example, a 1-piperazinyl group, a 4-methyl- 1-piperazinyl group, a 4-ethyl-l-piperazinyl group, a 4-isopropyl-l-piperazinyl group, a 4-tert- butyl- 1-piperazinyl group, a 4-cyclopropyl-l-piperazinyl group, a 4-cyclobutyl- 1-piperazinyl group, a 4-cyclopropylmethyl-l-piperazinyl group, a 4-(2-hydroxyethyl)- 1-piperazinyl group, a 4- (2-methoxyethyl)- 1-piperazinyl group, a 4-(2-methoxyacetyl)-l-piperazinyl group, a 4-acetyl-l- piperazinyl group, a 4-methylsulfonyl- 1-piperazinyl group, a 4-methyl-3-oxo-l-piperazinyl group, a 4-piperidyl group, a l-methyl-4-piperidyl group, a l-(2-hydroxyethyl)-4-piperidyl group, a 4- hydroxy-l-methyl-4-piperidyl group, more preferably a 4-methyl- 1-piperazinyl group, a 4-ethyl- l-piperazinyl group, a 4-(2-hydroxyethyl)- 1-piperazinyl group, a 4-acetyl-l- piperazinyl group, a l-methyl-4-piperidyl group.

R5 and Re are independently a hydrogen atom, a lower alkyl group or a hydroxy- lower alkyl group.

Preferred embodiments of R.5 and Ho are, for example, such that both of them are hydrogen atoms, or any one of them is a hydrogen atom and the other is a lower alkyl grou such as a methyl group and an ethyl group or a hydroxy-lower alkyl group such as a hydroxymethyl group and a 2-hydroxyethyl group.

In the compound of formula (I), R5₅ R6_? and Al may be at any substitutable position of the adjacent phenyl group.

The group of the formula:

is preferably a 4-(4-methyl-l-piperazinyl)phenyl group, a 3-methyl-4-(4-methyl-l- piperazinyl)phenyl group, a 3-hydroxymethyl-4-(4-methyl-l-piperazinyl)phenyl group, a 4-(4- ethyl-l-piperazinyl)phenyl group, a 4-(4-(2-hydroxyethyl)-l-piperazinyl)phenyl group, a 4-(4- acetyl-l-piperazinyl)phenyl group, a 4-(l-methyl-4-piperidyl)phenyl group.

The terms "any substitutable position" mean positions having substitutable hydrogen(s) on carbon, nitrogen, oxygen and/or sulfur atom(s) where the substitution of hydrogen is chemically allowed and the substitution results in a stable compound.

In the compounds of the invention, the replacement for methylene group(s) constituting the lower alkylene group by various radicals such as oxygen, sulfur, sulfinyl, sulfonyl, carbonyl, vinylene, and substituted or unsubstituted imine is allowed in case that the replacement is chemically allowed and the replacement results in a stable compound.

Depending on the type of the substituent and the salt form thereof, the compounds of the invention may be in the form of stereoisomers and tautomers such as optical isomers, diastereomers, geometrical isomers; and the compounds of the invention include all those stereoisomers and tautomers and their mixtures.

The invention includes various crystals, amorphous forms, salts, hydrates and solvates of the compounds of the invention. Further, prodrugs of the compounds of the invention are within the scope of the invention.

Examples of the compounds of formula (I) and their salts are, for example, the compounds and their salts described in Examples; and more preferred are the following compounds:

3-(2-allyl-6-{[4-(4-methylpiperazin-l-yl)phenyl]amino}-3-oxo-l,2-dihydro-3H- pyrazolo[3,4-d]pyrimidin-l-yl)-N,N-dimethylbenzamide,

2-allyl-6-{[3-(hydroxymethyl)-4-(4-methylpiperazin-l-yl)phenyl]amino}-l-(3- thienyl)-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

2-allyl- 1 - [3-(l -hydroxy- 1 -methylethyl)phenyl] -6- { [4-(4-methylpiperazin- 1 - yl)phenyl] amino} - 1 ,2-dihydro-3H-pyrazolo [3 ,4-d]pyrimidin-3 -one,

2-allyl- 1 - [3-(dimethylaminomethyl)phenyl] -6- { [4-(4-methylpiperazin- 1 - yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

2-allyl-6- { [3-hydroxymethyl-4-(4-methylpiperazin- 1 -yl)phenyl] amino} - 1 -pyridin- 2-yl-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

2-allyl-l-(6-aminopyridin-2-yl)-6-[{4-(4-methylpiperazin-l-yl)phenyl]amino}- l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

2-allyl- 1 - [6-(l -hydroxy- 1 -methylethyl)pyridin-2-yl] -6-{ [4-(4-methylpiperazin- 1 - yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

2-allyl-6-{[4-(4-ethylpiperazin-l-yl)phenyl]amino}-l-[6-(l-hydroxy-l- methylethyl)pyridin-2-yl]-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

6- { [4-(4-acetylpiperazin- l-yl)phenyl] amino} -2-allyl- 1 - [6-(l-hydroxy- 1 - methylethyl)pyridin-2-yl]-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

2-allyl-6-({4-[4-(2-hydroxyethyl)piperazin-l-yl]phenyl}amino)-l-[6-(l-hydroxy- l-methylethyl)pyridin-2-yl]-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

2-allyl-l-[6-(2-hydroxy-2-methylpropyl)pyridin-2-yl]-6-{[4-(l-methylpiperidin-4- yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

2-allyl-6-{[4-(4-methylpiperazin-l-yl)phenyl]amino}-l-[6-(2-oxopyrrolidin-l- yl)pyridin-2-yl]-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

N-{[6-(2-allyl-6-{[4-(4-methylpiperazin-l-yl)phenyl]amino}-3-oxo-l,2-dihydro- 3H-pyrazolo[3,4-d]pyrimidin-l-yl)pyridin-2-yl]methyl}-N-methylmethanesulfonamide,

1 - [6-(l -hydroxy- 1 -methylethyl)pyridin-2-yl] -6-{ [4-(4-methylpiperazin- 1 - yl)phenyl]amino}-2-(2-propynyl)-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one, and 2-allyl-l-[6-(3-methyl-2-oxoimidazolidm-l-yl)pyridin-2-yl]-6-{[4-(4- methylpiperazin-l-yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one.

Methods for producing the compounds of the invention are described below.

Compounds (I) of the invention may be produced, for example, according to the production methods mentioned below or according to the methods shown in Examples and Production Examples. However, the production methods for compounds (I) of the invention should not be limited to those reaction examples. Production Method 1

A compound of a general formula (II):

wherein LX is a leaving group; Rip is a lower alkenyl group or a lower alkynyl group; R.2p is a phenyl, pyridyl or thienyl group, which may have a group of -Q4p-A4p(Rlgp)Rlhp; Q4p _{1S a} single bond or a lower alkylene group, wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom or an optionally-protected carbonyl group, and/or substituted by a lower alkyl group; RlgP and Rlhp are independently a hydrogen atom, a halogen atom, a cyano group, an optionally-protected hydroxyl group, a lower alkyl group, a lower alkoxy-lower alkyl group, a lower alkanoyl group, a lower alkoxycarbonyl group or a lower alkylsulfonyl group, or together form a lower alkylene group wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom, a sulfur atom, a sulfinyl group, a sulfonyl group, an optionally-protected carbonyl group or a group of -N(RUp)-, and/or substituted by a halogen atom or a lower alkyl group, is reacted with a compound of a general formula (III) or its salt:

wherein Alp is selected from the following formula (aapl):

Rlcp is a hydrogen atom, a lower alkenyl group, or a group of -Q3p-A3p(Rldp)Rlep; ^3p is a nitrogen atom, or is a methine group or a l-vinyl-2-ylidene group which may be substituted by an optionally-protected hydroxyl group, a lower alkyl group or an optionally-protected hydroxy- lower alkyl group; Q3p is a single bond or a lower alkylene group, wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom, a sulfur atom, an optionally-protected carbonyl group, a sulfinyl group or a sulfonyl group, and/or substituted by a halogen atom, a cyano group, an optionally-protected hydroxyl group or a lower alkyl group; Rlφ and Rlep are independently a hydrogen atom, a halogen atom, a cyano group, an optionally-protected hydroxyl group, a lower alkyl group or an optionally-protected hydroxy-lower alkyl group, or together form a lower alkylene group wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom, a sulfur atom, a sulfinyl group, a sulfonyl group, an optionally-protected carbonyl group, a vinylene group or a group of -N(Rlφ)-, and/or substituted by an optionally-protected hydroxyl group or a lower alkyl group; Rlfp is an imino-protective group, a hydrogen atom, a lower alkyl group, a halo-lower alkyl group, a lower alkenyl group or a lower alkanoyl group; R5p and R6ρ are independently a hydrogen atom, a lower alkyl group or an optionally-protected hydroxy-lower alkyl group, to give a compound of a general formula

wherein Alp, Rip, R2p, R5p and R6p have the same meanings as above, and optionally the protective group is removed from it to produce a compound of a general formula (I):

wherein Al, Rl, R2, R5 and R6 have the same meanings as above.

The leaving group for Ll includes, for example, a halogen atom such as a chlorine atom, a bromine atom, an iodine atom; an organic sulfonyl group such as a methylsulfinyl group, a methylsulfonyl group, an ethylsulfonyl group, a phenylsulfonyl group; and an organic sulfonyloxy group such as a methylsulfonyloxy group, a trifluoromethylsulfonyloxy group, a p- tolylsulfonyloxy group; preferably a chlorine atom, a methylsulfinyl group, a methylsulfonyl group.

This production method is a general method for producing the compounds of formula (I).

In the above reaction, when the reactants have an amino group, an imino group, a hydroxyl group, a carboxyl group, a carbonyl group or the like that does not participate in the reaction, then the amino group, the imino group, the hydroxyl group, the carboxyl group and the carbonyl group may be suitably protected with an amino or imino-protective group, a hydroxyl- protective group, a carboxyl-protective group or a carbonyl-protective group, and thereafter the reactants may be reacted, and after the reaction, the protective group may be removed.

Not specifically defined, "amino or imino-protective group" may be any one having its function. For example, it includes an aralkyl group such as a benzyl group, a p- methoxybenzyl group, a 3,4-dimethoxybenzyl group, an o-nitrobenzyl group, a p-nitrobenzyl group, a benzhydryl group, a trityl group; a lower alkanoyl group such as a formyl group, an acetyl group, a propionyl group, a butyryl group, a pivaloyl group; a benzoyl group; an arylalkanoyl group such as a phenylacetyl group, a phenoxyacetyl group; a lower alkoxycarbonyl group such as a methoxycarbonyl group, an ethoxycarbonyl group, a propyloxycarbonyl group, a tert-butoxycarbonyl group; an aralkyloxycarbonyl group such as a benzyloxycarbonyl group, a p- nitrobenzyloxycarbonyl group, a phenethyloxycarbonyl group; a lower alkylsilyl group such as a trimethylsilyl group, a tert-butyldimethylsilyl group; a tetrahydropyranyl group; a trimethylsilylethoxymethyl group; a lower alkylsulfonyl group such as a methylsulfonyl group, an ethylsulfonyl group; an arylsulfonyl group such as benzenesulfonyl group, a toluenesulfonyl group; and is especially preferably an acetyl group, a benzoyl group, a tert-butoxycarbonyl group, a trimethylsilylethoxymethyl group, a methylsulfonyl group.

Not specifically defined, "hydroxyl-protective group" may be any one having its function. For example, it includes a lower alkyl group such as a methyl group, an ethyl group, a propyl group, an isopropyl group, a tert-butyl group; a lower alkylsilyl group such as a trimethylsilyl group, a tert-butyldimethylsilyl group; a lower alkoxymethyl group such as a methoxymethyl group, a 2-methoxyethoxymethyl group; a tetrahydropyranyl group; a trimethylsilylethoxymethyl group; an aralkyl group such as a benzyl group, a p-methoxybenzyl group, a 2,3-dimethoxybenzyl group, an o-nitrobenzyl group, a p-nitrobenzyl group, a trityl group; an acyl group such as a formyl group, an acetyl group; and is especially preferably a methyl group, a methoxymethyl group, a tetrahydropyranyl group, a trityl group, a trimethylsilylethoxymethyl group, a tert-butyldimethylsilyl group, an acetyl group.

Not specifically defined, "carboxyl-protective group" may be any one having its function. For example, it includes a lower alkyl group such as a methyl group, an ethyl group, a propyl group, an isopropyl group, a tert-butyl group; a halo-lower alkyl group such as a 2,2,2- trichloroethyl group; a lower alkenyl group such as an allyl group; an aralkyl group such as a benzyl group, a p-methoxybenzyl group, a p-nitrobenzyl group, a benzhydryl group, a trityl group; and is especially preferably a methyl group, an ethyl group, a tert-butyl group, an allyl group, a benzyl group, a p-methoxybenzyl group, a benzhydryl group.

Not specifically defined, "carbonyl-protective group" may be any one having its function. For example, it includes acetals and ketals such as ethylene ketal, trimethylene ketal, dimethylene ketal.

For the reaction of the compound of formula (II) and the compound of formula (III), in general, an equimolar or excessive molar amount, preferably from an equimolar amount to 1.5 mols of the compound (DI) is used relative to one mol of the compound (II).

The reaction is attained generally in an inert solvent. The inert solvent is, for example, preferably toluene, benzene, methylene chloride, chloroform, tetrahydrofuran, dioxane, dimethylformamide, N-methylpyrrolidone, dimethylsulfoxide and their mixed solvents.

Preferably, the reaction is attained in the presence of a base. The base includes, for example, organic bases such as triethylamine, diisopropylethylamine, pyridine, 4- dimethylaminopyridine; and inorganic bases such as sodium hydrogencarbonate, sodium carbonate, potassium carbonate, cesium carbonate, sodium hydroxide, potassium hydroxide.

The amount of the base to be used may be generally from an equimolar amount to an excessive molar amount, preferably from 1 to 3 mols relative to one mol of the compound of formula (II).

The reaction temperature may be generally from 0⁰C to 200⁰C, preferably from 20⁰C to 150°C.

The reaction time may be generally from 5 minutes to 7 days, preferably from 30 minutes to 24 hours.

After the reaction, the system may be processed in an ordinary manner to obtain a crude product of the compound of formula (IV). Thus obtained, the compound of formula (FV) is purified in an ordinary manner, or not purified, optionally it is processed for removing the protective group of the amino group, the hydroxyl group, the carboxyl group and the carbonyl group therein, optionally as suitably combined, thereby producing the compound of formula (I).

The method of removing the protective group varies, depending on the type of the protective group and on the stability of the intended compound (I). For example, the deprotection may be attained according to methods described in references [see Protective Groups in Organic Synthesis, 3rd. Ed., by T. W. Greene, John Wiley & Sons (1999)] or according to methods similar thereto. For example, herein employable are a method of solvolysis with an acid or a base, which comprises processing the protected compound with from 0.01 mols to a large excessive amount of an acid, preferably trifluoroacetic acid, formic acid or hydrochloric acid, or with from an equimolar amount to a large excessive amount of a base, preferably potassium hydroxide or calcium hydroxide; and a method of chemical reduction with a metal hydride complex, or catalytic reduction with a palladium-carbon catalyst or a Raney nickel catalyst.

The compounds of formula (I) may be readily isolated and purified in any ordinary separation method. Examples of the method are, for example, solvent extraction, recrystallization, column chromatography, preparative thin-layer chromatography.

The compounds may be converted into their pharmaceutically-acceptable salts or esters in an ordinary manner; and on the contrary, their salts or esters may also be converted into free compounds in an ordinary manner.

"Salts" of the compound of formula (III) mean ordinary salts used in the field of organic chemistry. For example, when the compound has an amino group or a basic heterocyclic group, then its salt are acid-addition salts at the amino group or the basic heterocyclic group.

The acid-addition salts include, for example, inorganic acid salts such as hydrochlorides, sulfates, nitrates, phosphates, perchlorates; organic acid salts such as maleates, fumarates, tartrates, citrates, ascorbates, trifluoroacetates; sulfonates such as methanesulfonates, isethionates, benzenesulfonates, p-toluenesulfonates.

The compounds of formulae (II) and (HI) may be commercially available, or may be produced according to methods described in references [see WO2006/004040, WO2003/037872; Journal of Medicinal Chemistry, Vol. 48, pp. 2371-2387; Bioorg. & Med. Chem. Lett., Vol. 14, pp. 5793-5797; Journal of the Chemical Society, Perkin Transaction II, Vol. 3, p. 843] or according to methods similar thereto, or according to the methods described below, or according to the methods described in Examples and Production Examples, optionally as suitably combined. Production Method A

( 1 ) ( 3 )

( 5 ) ( «1-1 )

wherein Et is an ethyl group; L2 is a leaving group; Me is a methyl group; Rip and R^p have the same meanings as above.

The production method A is a method for producing a compound of formula (II) where the leaving group for Ll is a methylsulfinyl group, or that is, a compound of formula (H-I).

According to this production method, the compound of formula (II- 1) can be produced by reacting a compound of formula (1) and a hydrazine derivative of formula (2) in the presence of a base to give a compound of formula (3), and thereafter introducing a group of Rip into the compound (3) to give a compound (5), and finally oxidizing the methylthio group in the compound (5) into a methylsulfinyl group.

In the step of reacting the compound of formula (1) and the hydrazine derivative of formula (2) in the presence of a base to give the compound of formula (3), in general, from 0.5 mols to an excessive molar amount, preferably from an equimolar amount to 3.0 mols of the hydrazine derivative (2) is used relative to one mol of the compound (1).

In general, the reaction is attained in an inert solvent. The inert solvent is, for example, preferably methylene chloride, chloroform, tetrahydrofuran, ethyl ether, benzene, toluene, dimethylformamide, or their mixed solvents.

Preferably, the reaction is attained in the presence of a base. The base includes, for example, organic bases such as triethylamine, diisopropylethylamine, pyridine, 4- dimethylaminopyridine; inorganic bases such as sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium hydrogencarbonate.

In general, the amount of the base to be used is preferably from an equimolar amount to an excessive molar amount relative to one mol of the compound (1). When the base is liquid, then the base may serve also as a solvent. The reaction temperature may be generally from -78°C to 100⁰C, preferably from 2O⁰C to 80⁰C.

In the step of reacting the compound (3) and the compound (4) to give the compound (5), in general, from 0.5 mols to an excessive molar amount, preferably from 2.0 mols to 5.0 mols of the compound (4) is used relative to one mol of the compound (3).

The leaving group for L2 is preferably a halogen atom such as a chlorine atom, a bromine atom, an iodine atom.

In general, the reaction may be attained in an inert solvent such as tetrahydrofuran, benzene, toluene, acetonitrile, dimethylformamide in the presence of a base such as sodium hydride, sodium amide, sodium alkoxide, or in a solvent such as methanol, ethanol, acetonitrile in the presence of a base such as sodium hydroxide, potassium hydroxide, potassium carbonate.

In general, the reaction temperature is preferably from 0⁰C to the boiling point of the solvent used in the reaction; and, in general, the reaction time is preferably from 1 hour to 48 hours.

To the step of oxidizing the methylthio group in the compound (5) to produce the compound (H-I), applicable is a method of oxidizing a methylthio group into a methylsulfinyl group or a methylsulfonyl group per se well known in the field of organic chemistry. In general, for example, in an inert solvent such as benzene, toluene, methylene chloride, chloroform, tetrahydrofuran, acetonitrile or dimethylformamide, from 0.5 mols to an excessive molar amount, preferably from an equimolar amount to 1.5 mols of an oxidizing agent such as metachloroperbenzoic acid or oxone may be used relative to one mol of the compound (5) for the oxidization.

The reaction temperature is, in general, preferably from 0⁰C to the boiling point of the solvent used in the reaction; and, in general, the reaction time is preferably from 30 minutes to 8 hours.

The compounds of formulae (1) and (2) may be commercially available, or may be produced according to known methods or according to the methods described in Examples, or according to methods similar thereto, optionally as suitably combined. Production Method B

wherein M is an ordinary organic metal atom; RP is a hydrogen atom, or an imino-protective group; Et, M, Me, Rip and R2p have the same meanings as above.

The imino-protective group for RP is, for example, preferably a benzyl group, a paramethoxybenzyl group, a tert-butoxycarbonyl group, a benzyloxycarbonyl group.

The production method B is a method for producing a compound of formula (II-l).

According to this production method, the compound of formula (II-l) can be produced by reacting a compound of formula (1) and a hydrazine derivative of formula (8) in the presence of a base, then hydrolyzing the resulting compound and cyclizing it to give a compound of formula (9), and thereafter reacting the compound (9) with an organic metal compound of formula (10) in the presence of a catalyst to thereby introduce a group of R2p thereinto to give a compound (5), and finally oxidizing the methylthio group in the compound (5) into a methylsulfonyl group.

In the step of reacting the compound of formula (1) and the hydrazine derivative of formula (8) in the presence of a base, in general, the amount of the hydrazine derivative (8) to be used may be from 0.5 mols to an excessive molar amount, preferably from an equimolar amount to 1.5 mols relative to one mol of the compound (1).

The reaction may be attained generally in the presence of an organic base such as triethylamine, diisopropylethylamine, pyridine, 4-dimethylaminopyridine, or an inorganic base such as sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium hydrogencarbonate, in an inert solvent such as methylene chloride, chloroform, tetrahydrofuran, ethyl ether, benzene, toluene, dimethylformamide, or their mixed solvents. In general, the amount of the base to be used is preferably from an equimolar amount to an excessive molar amount relative to one mol of the compound (1). When the base is liquid, the base may serve also as a solvent.

The reaction temperature may be generally from -78°C to 200⁰C, preferably from 20⁰C to 100⁰C.

The reaction time may be generally from 5 minutes to 7 days, preferably from 8 hours to 24 hours.

To the step of hydrolyzing the compound obtained in the above reaction, applicable is a method of hydrolysis of carboxylates per see well known in the field of organic chemistry. In general, in a solvent such as methanol, ethanol, tetrahydrofuran, dioxane, water or in their mixed solvent, the compound may be processed with an acid such as hydrochloric acid or sulfuric acid, or a base such as sodium hydroxide, potassium hydroxide or calcium hydroxide.

In general, the reaction temperature is preferably from 50⁰C to the boiling point of the solvent used in the reaction; and in general, the reaction time is preferably from 1 hour to 48 hours.

After the hydrolysis, the resulting compound is cyclized to produce the compound (9). For this, the reaction liquid may be made acidic after the hydrolysis, whereupon the cyclization may go on as such. In case where the cyclization does not go on, then the hydrolyzed compound may be refluxed under heat in the presence of acetic anhydride, or the hydrolyzed compound may be processed with thionyl chloride to attain the intended cyclization of the compound.

In the cyclization with acetic anhydride, the amount of acetic anhydride to be used is preferably an excessive molar amount, and the reaction time is, in general, preferably from 1 hour to 48 hours.

In case where the hydrolyzed compound is processed with thionyl chloride, the amount of thionyl chloride to be used is preferably an excessive molar amount, and the reaction time is, in general, preferably from 1 hour to 48 hours.

The step of reacting the compound (9) with the organic metal compound of formula (10) in the presence of a catalyst to thereby introduce a group of R2p thereinto to produce the compound (5) may be attained, using a halide compound having a group of R.2p in place of the organic metal compound of formula (10). When such a halide compound is used, then the catalyst is preferably a copper(I) iodide-diamine complex.

The step of oxidizing the methylthio group in the compound (5) to produce the compound (H-I) may be attained in the same manner as that for the step of oxidizing the methylthio group in the compound (5) to produce the compound (II-l) in the production method A. The compound of formula (8) may be commercially available, or may be produced according to known methods or according to the methods described in Examples, or according to methods similar thereto, optionally as suitably combined.

The pharmaceutical test examples for the compounds of the invention are shown below. Pharmaceutical Test 1 (Weel kinase-inhibitory effect)

(1) Purification of Weel kinase:

A cDNA of Weel kinase with glutathione-S-transferase (GST) fused at the amino terminal thereof was inserted into a baculovirus expression vector to construct a recombinant baculovirus, with which cells of an insect cell line Sf9 were infected for high expression therein. The infected cells were recovered and solubilized, and then the GST-tagged Weel kinase protein was adsorbed by a glutathione column, and eluted from the column with glutathione, and the active fraction was desalted in a desalting column to give a purified enzyme.

(2) Determination of Weel kinase activity:

In determination of the Weel kinase activity, a synthetic peptide, Poly(Lys,Tyr) Hydrobromide (Lys:Tyr (4:1)) bought from Sigma was used as the substrate.

The amount of the reaction mixture was 21.1 μL; and the composition of the reaction buffer was 50 mM Tris-HCl buffer (pH 7.4)/10 mM magnesium chloride/1 mM dithiothreitol. The purified Weel kinase, 2.5 μg of the substrate peptide, 10 μM of non-labeled adenosine triphosphate (ATP) and 1 μCi of [γ-33p] -labeled ATP (2500 Ci/mmol or more) were added to it, and incubated at 30⁰C for 30 minutes. Next, 10 μL of 350 mM phosphate buffer was added to the reaction mixture to stop the reaction. The substrate peptide was adsorbed by a P81 paper filter 96-well plate, then washed a few times with 130 mM phosphate buffer, and its radioactivity was counted with a liquid scintillation counter. The [γ-33p]_iabeled ATP was bought from Amersham Bioscience.

To add the test compound to the reaction system, the compound was diluted with dimethylsulfoxide (DMSO) to prepare a series of dilutions. 1.1 μL of each dilution was added to the reaction system. As a control, 1.1 μL of DMSO was added to the reaction system.

As in Table 1, the compounds of the invention exhibit an excellent Weel- inhibitory activity. Table 1

Pharmaceutical Test 2 (tumor growth-inhibitory effect)

Human colon cancer cells WiDr (gotten from ATCC) were implanted into the subcutaneous area of the back of F344/N Jcl-rnu nude rats. Eight days after the implantation, gemcitabine (50 mg/kg, Gemzar injection, Eli-Lilly) was intravenously administered to them; and after 24 hours, a test compound was dissolved in a solvent (5 % glucose) and given to them through continuous intravenous injection for 8 hours. The tumor volume (0.5 x (major diameter) x (minor diameter)2) was determined on day 0, 3, 6, 10 and 13. Day 0 means the day on which gemcitabine was administered. The relative tumor volume is a relative value, as calculated on the basis of the tumor volume of 1 on day 0. The tumor growth percentage (%T/C) was obtained according to the following formula:

When the tumor volume change from day 0 in the group subjected to test compound administration is more than 0 (> 0):

%T/C = [(tumor volume change in the test compounds on day 3, 6, 10, 13)/(tumor volume change in the control on day 3, 6, 10, 13)] x 100.

When the tumor volume change from day 0 in the group subjected to test compound administration is less than 0 (< 0):

%T/C = [(tumor volume change in the test compounds on day 3, 6, 10, 13)/(tumor volume change in the test compounds on day O)] x 100.

The data of the tumor growth-inhibiting effect are shown in Table 2.

Table 2

Gemcitabine administration reduced the tumor growth percentage, but when gemcitabine is combined with the compound of the invention, then the tumor growth percentage was further reduced. In particular, in the group where the chemical dose was high, the animals showed tumor involution.

As mentioned above, the compound of the invention in combination with other anticancer agent augmented the effect of the other anticancer agent. Pharmaceutical Test 3 (method of determining drug potency with cells (radiation (X-ray) sensitizing effect)) a) Reagents:

Fetal bovine serum (FBS) was gotten from Morgate; RPMI 1640 medium and 0.25 % trypsin EDTA were from Invitrogen; cycle test plus DNA reagent kit was from Becton Dickinson; and nylon net filter was from Millipore. b) Cells:

Human non-small-cell lung cancer cells (NCI-H1299) were gotten from ATCC. c) Method of effect determination:

NCI-H1299 cells were suspended in 10 % FBS-added RPMI 1640 medium, and the cell suspension was applied to a 6-well Nunclondelta-processed plastic plate bought from Nunc, in an amount of 100,000 cell/2 ml/well, and incubated overnight in 5 % CO2-95 % air at

37°C. Using Softex's M-150WE, the cells were irradiated with 5000 R X-rays, and then further incubated in 5 % CO2-95 % air at 37°C for 16 hours. A test compound was stepwise diluted with DMSO, and applied to a plate with the X-ray-processed cells sowed thereon, in an amount of 2 μL. This was incubated in 5 % CO2-95 % air at 37°C for 8 hours, and then the culture was partly taken out. 0.25 % trypsin was added to the cells remaining on the plate, in an amount of 600 μL, and statically kept at room temperature to prepare a single cell suspension. The single cell suspension and the previously-taken culture were mixed for every sample, then centrifuged, and the supernatant was removed. Sampling was thus completed. The sample was suspended in a buffer (1 mL) of cycle test plus DNA reagent kid, and frozen and stored at -80⁰C. The stored sample was thawed on the test date, centrifuged and the supernatant was removed, and this was suspended in cycle test plus A solution (250 μL), left statically at room temperature for 10 minutes, and then B solution (150 μL) was added thereto and further kept statically at room temperature for 10 minutes. Next, C solution (150 μL) was added to it, kept statically at 4°C for 10 minutes, and then filtered through nylon net filter to thereby complete DNA staining. Using Becton Dickinson's FACS Calibur, the DNA amount in each cell was quantitatively determined according to a FACS process, and the ratio of the cells having caused DNA fragmentation was determined.

Table 3

As in Table 3, the compound of the invention has an excellent DNA fragmentation-inducing effect to human-derived cancer cells (NCI-H1299).

As mentioned above, the compound of the invention in combination with X-ray augmented the effect of the X-ray.

The compounds of formula (I) can be administered orally or parenterally, and after formulated into preparations suitable to such administration modes, the compounds can be used as pharmaceutical compositions and anticancer agents.

The term "cancer" as referred to in this description includes various sarcoma and carcinoma and includes solid cancer and hematopoietic cancer. The solid cancer as referred to herein includes, for example, brain tumor, cervicocerebral cancer, esophageal cancer, thyroid cancer, small cell cancer, non-small cell cancer, breast cancer, lung cancer, stomach cancer, gallbladder/bile duct cancer, liver cancer, pancreatic cancer, colon cancer, rectal cancer, ovarian cancer, choriocarcinoma, uterus body cancer, uterocervical cancer, renal pelvis/ureter cancer, bladder cancer, prostate cancer, penis cancer, testicles cancer, fetal cancer, Wilms' tumor, skin cancer, malignant melanoma, neuroblastoma, osteosarcoma, Ewing's tumor, soft part sarcoma. On the other hand, the hematopoietic cancer includes, for example, acute leukemia, chronic lymphatic leukemia, chronic myelocytic leukemia, polycythemia vera, malignant lymphoma, multiple myeloma, Hodgkin's lymphoma, non-Hodgkin's lymphoma.

The term "treatment of cancer" as referred to in this description means that an anticancer agent is administered to a cancer case so as to inhibit the growth of the cancer cells in the case. Preferably, the treatment results in cancer growth regression, or that is, it reduces the size of a detectable cancer. More preferably, the treatment results in complete disappearance of cancer.

The compounds of the invention are expected to be effective especially to human solid cancer. The human solid cancer includes, for example, brain cancer, cervicocerebral cancer, esophageal cancer, thyroid cancer, small cell cancer, non-small cell cancer, breast cancer, lung cancer, stomach cancer, gallbladder/bile duct cancer, liver cancer, pancreatic cancer, colon cancer, rectal cancer, ovarian cancer, choriocarcinoma, uterus body cancer, uterocervical cancer, renal pelvis/ureter cancer, bladder cancer, prostate cancer, penis cancer, testicles cancer, fetal cancer, Wilms' cancer, skin cancer, malignant melanoma, neuroblastoma, osteosarcoma, Ewing's tumor, soft part sarcoma, acute leukemia, chronic lymphatic leukemia, chronic myelocytic leukemia, Hodgkin's lymphoma.

The pharmaceutical composition and anticancer agent of the invention may contain a pharmaceutically acceptable carrier or diluent. Here, the "pharmaceutically acceptable carrier or diluent" refers to excipients [e.g., fats, beeswax, semi-solid and liquid polyols, natural or hydrogenated oils, etc.]; water (e.g., distilled water, particularly distilled water for injection, etc.), physiological saline, alcohol (e.g., ethanol), glycerol, polyols, aqueous glucose solution, mannitol, plant oils, etc.); additives [e.g., extending agent, disintegrating agent, binder, lubricant, wetting agent, stabilizer, emulsifier, dispersant, preservative, sweetener, colorant, seasoning agent or aromatizer, concentrating agent, diluent, buffer substance, solvent or solubilizing agent, chemical for achieving storage effect, salt for modifying osmotic pressure, coating agent or antioxidant], and the like.

With regard to each preparation of the pharmaceutical composition and anticancer agent of the invention, various preparation forms can be selected, and examples thereof include oral preparations such as tablets, capsules, powders, granules or liquids, or sterilized liquid parenteral preparations such as solutions or suspensions, suppositories, ointments and the like.

Solid preparations can be prepared in the forms of tablet, capsule, granule and powder without any additives, or prepared using appropriate carriers (additives). Examples of such carriers (additives) may include saccharides such as lactose or glucose; starch of corn, wheat or rice; fatty acids such as stearic acid; inorganic salts such as magnesium metasilicate aluminate or anhydrous calcium phosphate; synthetic polymers such as polyvinylpyrrolidone or polyalkylene glycol; alcohols such as stearyl alcohol or benzyl alcohol; synthetic cellulose derivatives such as methylcellulose, carboxymethylcellulose, ethylcellulose or hydroxypropylmethylcellulose; and other conventionally used additives such as gelatin, talc, plant oil and gum arabic.

These solid preparations such as tablets, capsules, granules and powders may generally contain, for example, 0.1 to 100% by weight, and preferably 5 to 98% by weight, of the compound of the above Formula (I) as an active ingredient, based on the total weight of the preparation.

Liquid preparations are produced in the forms of suspension, syrup, injection and drip infusion (intravenous fluid) using appropriate additives that are conventionally used in liquid preparations, such as water, alcohol or a plant-derived oil such as soybean oil, peanut oil and sesame oil.

In particular, when the preparation is administered parenterally in a form of intramuscular injection, intravenous injection or subcutaneous injection, appropriate solvent or diluent may be exemplified by distilled water for injection, an aqueous solution of lidocaine hydrochloride (for intramuscular injection), physiological saline, aqueous glucose solution, ethanol, polyethylene glycol, propylene glycol, liquid for intravenous injection (e.g., an aqueous solution of citric acid, sodium citrate and the like) or an electrolytic solution (for intravenous drip infusion and intravenous injection), or a mixed solution thereof.

Such injection may be in a form of a preliminarily dissolved solution, or in a form of powder per se or powder associated with a suitable carrier (additive) which is dissolved at the time of use. The injection liquid may contain, for example, 0.1 to 10% by weight of an active ingredient based on the total weight of the preparation.

Liquid preparations such as suspension or syrup for oral administration may contain, for example, 0.1 to 10% by weight of an active ingredient based on the total weight of the preparation.

The preparation can be prepared by a person having ordinary skill in the art according to conventional methods or common techniques. For example, a preparation can be carried out, if the preparation is an oral preparation, for example, by mixing an appropriate amount of the compound of the invention with an appropriate amount of lactose and filling this mixture into hard gelatin capsules which are suitable for oral administration. On the other hand, preparation can be carried out, if the preparation containing the compound of the invention is an injection, for example, by mixing an appropriate amount of the compound of the invention with an appropriate amount of 0.9% physiological saline and filling this mixture in vials for injection.

The compounds of the invention may be sued, optionally as combined with any other agent useful for treatment of various cancers or with radiotherapy. The individual ingredients for such combination may be administered at different times or at the same time as divided preparations or one preparation during the term of treatment. Accordingly, the invention should be so interpreted that it includes all modes of administration at the same time or at different times, and the administration in this invention should be interpreted so. The scope of the combination of the compound of the invention and any other agent useful for the above- mentioned diseases should include, in principle, any and every combination thereof with any and every pharmaceutical agent useful for the treatment of the above-mentioned diseases.

Radiation therapy itself means an ordinary method in the field of treatment of cancer. For radiation therapy, employable are various radiations such as X-ray, γ-ray, neutron ray, electron beam, proton beam; and radiation sources. In a most popular radiation therapy, a linear accelerator is used for irradiation with external radiations, γ-ray.

The compounds of the invention may be combined with radiation therapy to enhance the therapeutical effect in radiation therapy; and the compounds may be therefore useful as a radiation sensitizer in the field of treatment of cancer.

Another aspect of the compounds of the invention is that the compounds are also useful as a sensitizer for any other anticancer agents in the field of treatment of cancer. The compounds of the invention may be combined with radiation therapy and/or combined with any other anticancer agents described below in their use for treatment of cancer.

"Sensitizer" for radiation therapy or anticancer agent as referred to herein is meant to indicate a medical agent which, when used as combined with radiation therapy and/or chemotherapy with an anticancer agent, may additively or synergistically augment the therapeutical effect of that radiation therapy and/or chemotherapy.

The agents to be in the combined preparations in the invention may have any forms selected in any manner, and they may be produced in the same manner as that for the above-mentioned preparations. The combined agent comprising the compound of the invention and some other anticancer agent may be readily produced by anyone skilled in the art according to ordinary methods or conventional techniques.

The above-mentioned combination includes not only the compositions of the invention that contain one other active substance but also those containing two or more other active substances. There are a lot of examples of the combination of the composition of the invention and one or two or more active substances selected from the remedies for the above- mentioned diseases.

The agents to be combined with the compositions include, for example, an anticancer agent selected from the group consisting of anticancer alkylating agents, anticancer antimetabolites, anticancer antibiotics, plant-derived anticancer agents, anticancer platinum coordination compounds, anticancer camptothecin derivatives, anticancer tyrosine kinase inhibitors, monoclonal antibodies, interferons, biological response modifiers and other anticancer agents as well as pharmaceutically acceptable salt(s) or ester(s) thereof.

The term "anticancer alkylating agent" as used in the present specification refers to an alkylating agent having anticancer activity, and the term "alkylating agent" herein generally refers to an agent giving an alkyl group in the alkylation reaction in which a hydrogen atom of an organic compound is substituted with an alkyl group. The term "anticancer alkylating agent" may be exemplified by nitrogen mustard N-oxide, cyclophosphamide, ifosfamide, melphalan, busulfan, mitobronitol, carboquone, thiotepa, ranimustine, nimustine, temozolomide or carmustme.

The term "anticancer antimetabolite" as used in the specification refers to an antimetabolite having anticancer activity, and the term "antimetabolite" herein includes, in a broad sense, substances which disturb normal metabolism and substances which inhibit the electron transfer system to prevent the production of energy-rich intermediates, due to their structural or functional similarities to metabolites that are important for living organisms (such as vitamins, coenzymes, amino acids and saccharides). The term "anticancer antimetabolites" may be exemplified methotrexate, 6-mercaptopurine riboside, mercaptopurine, 5-fluorouracil, tegafur, doxifluridine, caxmofur, cytarabine, cytarabine ocfosfate, enocitabine, S-I, gemcitabine, fhidarabine or pemetrexed disodium, and preferred are cytarabine, gemcitabine and the like.

The term "anticancer antibiotic" as used in the specification refers to an antibiotic having anticancer activity, and the "antibiotic" herein includes substances that are produced by microorganisms and inhibit cell growth and other functions of microorganisms and of other living organisms. The term "anticancer antibiotic" may be exemplified by actinomycin D, doxorubicin, daunorubicin, neocarzinostatin, bleomycin, peplomycin, mitomycin C, aclarubicin, pirarubicin, epirubicin, zinostatin stimalamer, idarubicin, sirolimus or valrubicin, and preferred are doxorubicin, mitomycin C and the like.

The term "plant-derived anticancer agent" as used in the specification includes compounds having anticancer activities which originate from plants, or compounds prepared by applying chemical modification to the foregoing compounds. The term "plant-derived anticancer agent" may be exemplified by vincristine, vinblastine, vindesine, etoposide, sobuzoxane, docetaxel, paclitaxel and vinorelbine, and preferred are etoposide and the like.

The term "anticancer camptothecin derivative" as used in the specification refers to compounds that are structurally related to camptothecin and inhibit cancer cell growth, including camptothecin per se. The term "anticancer camptothecin derivative" is not particularly limited to, but may be exemplified by, camptothecin, 10-hydroxycamptothecin, topotecan, irinotecan or 9-aminocamptothecin, with camptothecin being preferred. Further, irinotecan is metabolized in vivo and exhibits anticancer effect as SN-38. The action mechanism and the activity of the camptothecin derivatives are believed to be virtually the same as those of camptothecin (e.g., Nitta, et al., Gan to Kagaku Ryoho, 14, 850-857 (1987)).

The term "anticancer platinum coordination compound" as used in the specification refers to a platinum coordination compound having anticancer activity, and the term "platinum coordination compound" herein refers to a platinum coordination compound which provides platinum in ion form. Preferred platinum compounds include cisplatin; cis- diamminediaquoplatinum (π)-ion; chloro(diethylenetriamme)-platinum (II) chloride; dichloro(ethylenediamine)-platinum (II); diammine(l,l-cyclobutanedicarboxylato) platinum (II) (carboplatin); spiroplatin; iproplatin; diammine(2-ethylmalonato)platinum (II); ethylenediaminemalonatoplatinum (II); aqua(l,2-diaminodicyclohexane)sulfatoplatinum (II); aqua(l,2-diaminodicyclohexane)malonatoplatinum (JI); (1,2- diaminocyclohexane)malonatoplatinum (π); (4-carboxyphthalato)(l,2-diaminocyclohexane) platinum (II); (l,2-diaminocyclohexane)-(isocitrato)platinum (II); (1,2- diaminocyclohexane)oxalatoplatinum (II); ormaplatin; tetraplatin; carboplatin, nedaplatin and oxaliplatin, and preferred is cisplatin. Further, other anticancer platinum coordination compounds mentioned in the specification are known and are commercially available and/or producible by a person having ordinary skill in the art by conventional techniques. The term "anticancer tyrosine kinase inhibitor" as used in the specification refers to a tyrosine kinase inhibitor having anticancer activity, and the term "tyrosine kinase inhibitor" herein refers to a chemical substance inhibiting "tyrosine kinase" which transfers a γ-phosphate group of ATP to a hydroxyl group of a specific tyrosine in protein. The term "anticancer tyrosine kinase inhibitor" may be exemplified by gefitinib, imatinib or erlotinib.

The term "monoclonal antibody" as used in the specification, which is also known as single clonal antibody, refers to an antibody produced by a monoclonal antibody-producing cell, and examples thereof include cetuximab, bevacizumab, rituximab, alemtuzumab and trastuzumab.

The term "interferon" as used in the specification refers to an interferon having anticancer activity, and it is a glycoprotein having a molecular weight of about 20,000 which is produced and secreted by most animal cells upon viral infection. It has not only the effect of inhibiting viral growth but also various immune effector mechanisms including inhibition of growth of cells (in particular, tumor cells) and enhancement of the natural killer cell activity, thus being designated as one type of cytokine. Examples of "interferon" include interferon α, interferon α-2a, interferon α-2b, interferon β, interferon γ-la and interferon γ-nl.

The term "biological response modifier" as used in the specification is the so- called biological response modifier or BRM and is generally the generic term for substances or drugs for modifying the defense mechanisms of living organisms or biological responses such as survival, growth or differentiation of tissue cells in order to direct them to be useful for an individual against tumor, infection or other diseases. Examples of the "biological response modifier" include krestin, lentinan, sizofiran, picibanil and ubenimex.

The term "other anticancer agent" as used in the specification refers to an anticancer agent which does not belong to any of the above-described agents having anticancer activities. Examples of the "other anticancer agent" include mitoxantrone, L-asparaginase, procarbazine, dacarbazine, hydroxycarbamide, pentostatin, tretinoin, alefacept, darbepoetin alfa, anastrozole, exemestane, bicalutamide, leuprorelin, flutamide, fulvestrant, pegaptanib octasodium, denileukin diftitox, aldesleukin, thyrotropin alfa, arsenic trioxide, bortezomib, capecitabine, and goserelin.

The above-described terms "anticancer alkylating agent", "anticancer antimetabolite", "anticancer antibiotic", "plant-derived anticancer agent", "anticancer platinum coordination compound", "anticancer camptothecin derivative", "anticancer tyrosine kinase inhibitor", "monoclonal antibody", "interferon", "biological response modifier" and "other anticancer agent" are all known and are either commercially available or producible by a person skilled in the art by methods known per se or by well-known or conventional methods. The process for preparation of gefitinib is described, for example, in USP No. 5,770,599; the process for preparation of cetuximab is described, for example, in WO 96/40210; the process for preparation of bevacizumab is described, for example, in WO 94/10202; the process for preparation of oxaliplatin is described, for example, in USP Nos. 5,420,319 and 5,959,133; the process for preparation of gemcitabine is described, for example, in USP Nos. 5,434,254 and 5,223,608; and the process for preparation of camptothecin is described in USP Nos. 5,162,532, 5,247,089, 5,191,082, 5,200,524, 5,243,050 and 5,321,140; the process for preparation of irinotecan is described, for example, in USP No. 4,604,463; the process for preparation of topotecan is described, for example, in USP No. 5,734,056; the process for preparation of temozolomide is described, for example, in JP-B No. 4-5029; and the process for preparation of rituximab is described, for example, in JP-W No. 2-503143.

The above-mentioned anticancer alkylating agents are commercially available, as exemplified by the following: nitrogen mustard N-oxide from Mitsubishi Pharma Corp. as Nitromin (tradename); cyclophosphamide from Shionogi & Co., Ltd. as Endoxan (tradename); ifosfamide from Shionogi & Co., Ltd. as Ifomide (tradename); melphalan from GlaxoSmithKline Corp. as Alkeran (tradename); busulfan from Takeda Pharmaceutical Co., Ltd. as Mablin (tradename); mitobronitol from Kyorin Pharmaceutical Co., Ltd. as Myebrol (tradename); carboquone from Sankyo Co., Ltd. as Esquinon (tradename); thiotepa from Sumitomo Pharmaceutical Co., Ltd. as Tespamin (tradename); ranimustine from Mitsubishi Pharma Corp. as Cymerin (tradename); nimustine from Sankyo Co., Ltd. as Nidran (tradename); temozolomide from Schering Corp. as Temodar (tradename); and carmustine from Guilford Pharmaceuticals Inc. as Gliadel Wafer (tradename).

The above-mentioned anticancer antimetabolites are commercially available, as exemplified by the following: methotrexate from Takeda Pharmaceutical Co., Ltd. as Methotrexate (tradename); 6-mercaptopurine riboside from Aventis Corp. as Thioinosine (tradename); mercaptopurine from Takeda Pharmaceutical Co., Ltd. as Leukerin (tradename); 5- fluorouracil from Kyowa Hakko Kogyo Co., Ltd. as 5-FU (tradename); tegafur from Taiho Pharmaceutical Co., Ltd. as Futraful (tradename); doxyfluridine from Nippon Roche Co., Ltd. as Furutulon (tradename); carmofur from Yamanouchi Pharmaceutical Co., Ltd. as Yamafur (tradename); cytarabine from Nippon Shinyaku Co., Ltd. as Cylocide (tradename); cytarabine ocfosfate from Nippon Kayaku Co., Ltd. as Strasid(tradename); enocitabine from Asahi Kasei Corp. as Sanrabin (tradename); S-I from Taiho Pharmaceutical Co., Ltd. as TS-I (tradename); gemcitabine from Eli Lilly & Co. as Gemzar (tradename); fludarabine from Nippon Schering Co., Ltd. as Fludara (tradename); and pemetrexed disodium from Eli Lilly & Co. as Alimta (tradename).

The above-mentioned anticancer antibiotics are commercially available, as exemplified by the following: actinomycin D from Banyu Pharmaceutical Co., Ltd. as Cosmegen (tradename); doxorubicin from Kyowa Hakko Kogyo Co., Ltd. as adriacin (tradename); daunorubicin from Meiji Seika Kaisha Ltd. as Daunomycin; neocarzinostatin from Yamanouchi Pharmaceutical Co., Ltd. as Neocarzinostatin (tradename); bleomycin from Nippon Kayaku Co., Ltd. as Bleo (tradename); pepromycin from Nippon Kayaku Co, Ltd. as Pepro (tradename); mitomycin C from Kyowa Hakko Kogyo Co., Ltd. as Mitomycin (tradename); aclarubicin from Yamanouchi Pharmaceutical Co., Ltd. as Aclacinon (tradename); pirarubicin from Nippon Kayaku Co., Ltd. as Pinorubicin (tradename); epirubicin from Pharmacia Corp. as Pharmorubicin (tradename); zinostatin stimalamer from Yamanouchi Pharmaceutical Co., Ltd. as Smancs (tradename); idarubicin from Pharmacia Corp. as Idamycin (tradename); sirolimus from Wyeth Corp. as Rapamune (tradename); and valrubicin from Anthra Pharmaceuticals Inc. as Valstar (tradename).

The above-mentioned plant-derived anticancer agents are commercially available, as exemplified by the following: vincristine from Shionogi & Co., Ltd. as Oncovin (tradename); vinblastine from Kyorin Pharmaceutical Co., Ltd. as Vinblastine (tradename); vindesine from Shionogi & Co., Ltd. as Fildesin (tradename); etoposide from Nippon Kayaku Co., Ltd. as Lastet (tradename); sobuzoxane from Zenyaku Kogyo Co., Ltd. as Perazolin (tradename); docetaxel from Aventis Corp. as Taxsotere (tradename); paclitaxel from Bristol-Myers Squibb Co. as Taxol (tradename); and vinorelbine from Kyowa Hakko Kogyo Co., Ltd. as Navelbine (tradename).

The above-mentioned anticancer platinum coordination compounds are commercially available, as exemplified by the following: cisplatin from Nippon Kayaku Co., Ltd. as Randa (tradename); carboplatin from Bristol-Myers Squibb Co. as Paraplatin (tradename); nedaplatin from Shionogi & Co., Ltd. as Aqupla (tradename); and oxaliplatin from Sanofi- Synthelabo Co. as Eloxatin (tradename).

The above-mentioned anticancer camptothecin derivatives are commercially available, as exemplified by the following: irinotecan from Yakult Honsha Co., Ltd. as Campto (tradename); topotecan from GlaxoSmithKline Corp. as Hycamtin (tradename); and camptothecin from Aldrich Chemical Co., Inc., U.S.A.

The above-mentioned anticancer tyrosine kinase inhibitors are commercially available, as exemplified by the following: gefitinib from AstraZeneca Corp. as Iressa (tradename); imatinib from Novartis AG as Gleevec (tradename); and erlotinib from OSI Pharmaceuticals Inc. as Tarceva (tradename).

The above-mentioned monoclonal antibodies are commercially available, as exemplified by the following: cetuximab from Bristol-Myers Squibb Co. as Erbitux (tradename); bevacizumab from Genentech, Inc. as Avastin (tradename); rituximab from Biogen Idee Inc. as Rituxan (tradename); alemtuzumab from Berlex Inc. as Campath (tradename); and trastuzumab from Chugai Pharmaceutical Co., Ltd. as Herceptin (tradename).

The above-mentioned interferons are commercially available, as exemplified by the following: interferon cc from Sumitomo Pharmaceutical Co., Ltd. as Sumiferon (tradename); interferon α-2a from Takeda Pharmaceutical Co., Ltd. as Canferon-A (tradename); interferon α- 2b from Schering-Plough Corp. as Intron A (tradename); interferon β from Mochida Pharmaceutical Co., Ltd. as IFNβ (tradename); interferon γ-la from Shionogi & Co., Ltd. as Imunomax-γ (tradename); and interferon γ-nl from Otsuka Pharmaceutical Co., Ltd. as Ogamma (tradename).

The above-mentioned biological response modifiers are commercially available, as exemplified by the following: krestin from Sankyo Co., Ltd. as krestin (tradename); lentinan from Aventis Corp. as Lentinan (tradename); sizofiran from Kaken Seiyaku Co., Ltd. as Sonifiran (tradename); picibanil from Chugai Pharmaceutical Co., Ltd. as Picibanil (tradename); and ubenimex from Nippon Kayaku Co., Ltd. as Bestatin (tradename).

The above-mentioned other anticancer agents are commercially available, as exemplified by the following: mitoxantrone from Wyeth Lederle Japan, Ltd. as Novantrone (tradename); L-asparaginase from Kyowa Hakko Kogyo Co., Ltd. as Leunase (tradename); procarbazine from Nippon Roche Co., Ltd. as Natulan (tradename); dacarbazine from Kyowa Hakko Kogyo Co., Ltd. as Dacarbazine (tradename); hydroxycarbamide from Bristol-Myers Squibb Co. as Hydrea (tradename); pentostatin from Kagaku Oyobi Kessei Ryoho Kenkyusho as Coforin (tradename); tretinoin from Nippon Roche Co., Ltd. As Vesanoid (tradename); alefacept from Biogen Idee Inc. as Amevive (tradename); darbepoetin alfa from Amgen Inc. as Aranesp (tradename); anastrozole from AstraZeneca Corp. as Arimidex (tradename); exemestane from Pfizer Inc. as Aromasin (tradename); bicalutamide from AstraZeneca Corp. as Casodex (tradename); leuprorelin from Takeda Pharmaceutical Co., Ltd. as Leuplin (tradename); flutamide from Schering-Plough Corp. as Eulexin (tradename); fulvestrant from AstraZeneca Corp. as Faslodex (tradename); pegaptanib octasodium from Gilead Sciences, Inc. as Macugen (tradename); denileukin diftitox from Ligand Pharmaceuticals Inc. as Ontak (tradename); aldesleukin from Chiron Corp. as Proleukin (tradename); thyrotropin alfa from Genzyme Corp. as Thyrogen (tradename); arsenic trioxide from Cell Therapeutics, Inc. as Trisenox (tradename); bortezomib from Millennium Pharmaceuticals, Inc. as Velcade (tradename); capecitabine from Hoffmann-La Roche, Ltd. as Xeloda (tradename); and goserelin from AstraZeneca Corp. as Zoladex (tradename).

The invention also relates to a method for the treatment of cancer, which comprises administering to a subject in need thereof a therapeutically-effective amount of the compound of the invention or its salt or ester thereof.

In the process according to the invention, preferred therapeutic unit may vary in accordance with, for example, the administration route of the compound of the invention, the type of the compound of the invention used, and the dosage form of the compound of the invention used; the type, administration route and dosage form of the other anticancer agent used in combination; and the type of cells to be treated, the condition of patient, and the like. The optimal treatment under the given conditions can be determined by a person skilled in the art, based on the set conventional therapeutic unit and/or based on the content of the present specification.

In the process according to the invention, the therapeutic unit for the compound of the invention may vary in accordance with, specifically, the type of compound used, the type of compounded composition, application frequency and the specific site to be treated, seriousness of the disease, age of the patient, doctor's diagnosis, the type of cancer, or the like. However, as an exemplary reference, the daily dose for an adult may be within a range of, for example, 1 to 1,000 mg in the case of oral administration. In the case of parenteral administration, preferably intravenous administration, and more preferably intravenous drip infusion, the daily dose may be within a range of, for example, 1 to 100 mg/m2 (body surface area). Here, in the case of intravenous drip infusion, administration may be continuously carried out for, for example, 1 to 48 hours. Moreover, the administration frequency may vary depending on the administering method and symptoms, but it is, for example, once to five times a day. Alternatively, periodically intermittent administration such as administration every other day, administration every two days or the like may be employed as well in the administering method. The period of withdraw from medication in the case of parenteral administration is, for example, 1 to 6 weeks.

Although the therapeutic unit for the other anticancer agent used in combination with the compound of the invention is not particularly limited, it can be determined, if needed, by those skilled in the art according to known literatures. Examples may be as follows.

The therapeutic unit of 5-fluorouracil (5-FU) is such that, in the case of oral administration, for example, 200 to 300 mg per day is administered in once to three times consecutively, and in the case of injection, for example, 5 to 15 mg/kg per day is administered once a day for the first 5 consecutive days by intravenous injection or intravenous drip infusion, and then 5 to 7.5 mg/kg is administered once a day every other day by intravenous injection or intravenous drip infusion (the dose may be appropriately increased or decreased).

The therapeutic unit of S-I (Tegafur, Gimestat and Ostat potassium) is such that, for example, the initial dose (singe dose) is set to the following standard amount in accordance with the body surface area, and it is orally administered twice a day, after breakfast and after dinner, for 28 consecutive days, followed by withdrawal from medication for 14 days. This is set as one course of administration, which is repeated. The initial standard amount per unit body surface area (Tegafur equivalent) is 40 mg in one administration for an area less than 1.25 m2; 50 mg in one administration for an area of 1.25 m2 to less than 1.5 m2; 60 mg in one administration for an area of 1.5 m2 or more. This dose is appropriately increased or decreased depending on the condition of the patient.

The therapeutic unit for gemcitabine is, for example, 1 g as gemcitabine/m2 in one administration, which is administered by intravenous drip infusion over a period of 30 minutes, and one administration per week is continued for 3 weeks, followed by withdrawal from medication on the fourth week. This is set as one course of administration, which is repeated. The dose is appropriately decreased in accordance with age, symptom or development of side- effects.

The therapeutic unit for doxorubicin (e.g., doxorubicin hydrochloride) is such that, for example, in the case of intravenous injection, 10 mg (0.2 mg/kg) (titer) is administered once a day by intravenous one-shot administration for 4 to 6 consecutive days, followed by withdrawal from medication for 7 to 10 days. This is set as one course of administration, which is repeated two or three times. Here, the total dose is preferably 500 mg (titer)/m2 (body surface area) or less, and it may be appropriately increased or decreased within the range.

The therapeutic unit for etoposide is such that, for example, in the case of intravenous injection, 60 to 100 mg/m2 (body surface area) per day is administered for 5 consecutive days, followed by withdrawal from medication for three weeks (the dose may be appropriately increased or decreased). This is set as one course of administration, which is repeated. Meanwhile, in the case of oral administration, for example, 175 to 200 mg per day is administered for 5 consecutive days, followed by withdrawal from medication for three weeks (the dose may be appropriately increased or decreased). This is set as one course of administration, which is repeated.

The therapeutic unit for docetaxel (docetaxel hydrate) is such that, for example, 60 mg as docetaxel/m2 (body surface area) is administered once a day by intravenous drip infusion over a period of 1 hour or longer at an interval of 3 to 4 weeks (the dose may be appropriately increased or decreased).

The therapeutic unit of paclitaxel is such that, for example, 210 mg/m2 (body surface area) is administered once a day by intravenous drip infusion over a period of 3 hours, followed by withdrawal from medication for at least 3 weeks. This is set as one course of administration, which is repeated. The dose may be appropriately increased or decreased.

The therapeutic unit for cisplatin is such that, for example, in the case of intravenous injection, 50 to 70 mg/m2 (body surface area) is administered once a day, followed by withdrawal from medication for 3 weeks or longer (the dose may be appropriately increased or decreased). This is set as one course of administration, which is repeated.

The therapeutic unit for carboplatin is such that, for example, 300 to 400 mg/m2 is administered once a day by intravenous drip infusion over a period of 30 minutes or longer, followed by withdrawal from medication for at least 4 weeks (the dose may be appropriately increased or decreased). This is set as one course of administration, which is repeated.

The therapeutic unit for oxaliplatin is such that 85 mg/m2 is administered once a day by intravenous injection, followed by withdrawal from medication for two weeks. This is set as one course of administration, which is repeated. The therapeutic unit for irinotecan (e.g., irinotecan hydrochloride) is such that, for example, 100 mg/m2 is administered once a day by intravenous drip infusion for 3 or 4 times at an interval of one week, followed by withdrawal from medication for at least two weeks.

The therapeutic unit for topotecan is such that, for example, 1.5 mg/m2 is administered once a day by intravenous drip infusion for 5 days, followed by withdrawal from medication for at least 3 weeks.

The therapeutic unit for cyclophosphamide is such that, for example, in the case of intravenous injection, 100 mg is administered once a day by intravenous injection for consecutive days. If the patient can tolerate, the daily dose may be increased to 200 mg. The total dose is 3,000 to 8,000 mg, which may be appropriately increased or decreased. If necessary, it may be injected or infused intramuscularly, intrathoracically or intratumorally. On the other hand, in the case of oral administration, for example, 100 to 200 mg is administered a day.

The therapeutic unit for gefitinib is such that 250 mg is orally administered once a day.

The therapeutic unit for cetuximab is such that, for example, 400 mg/m2 is administered on the first day by intravenous drip infusion, and then 250 mg/m2 is administered every week by intravenous drip infusion.

The therapeutic unit for bevacizumab is such that, for example, 3 mg/kg is administered every week by intravenous drip infusion.

The therapeutic unit for trastuzumab is such that, for example, typically for an adult, once a day, 4 mg as trastuzumab/kg (body weight) is administered initially, followed by intravenous drip infusion of 2 mg/kg over a period of 90 minutes or longer every week from the second administration.

The therapeutic unit for exemestane is such that, for example, typically for an adult, 25 mg is orally administered once a day after meal.

The therapeutic unit for leuprorelin (e.g., leuprorelin acetate) is such that, for example, typically for an adult, 11.25 mg is subcutaneously administered once in 12 weeks.

The therapeutic unit for imatinib is such that, for example, typically for an adult in the chronic phase of chronic myelogenous leukemia, 400 mg is orally administered once a day after meal.

The therapeutic unit for a combination of 5-FU and leucovorin is such that, for example, 425 mg/m2 of 5-FU and 200 mg/m2 of leucovorin are administered from the first day to the fifth day by intravenous drip infusion, and this course is repeated at an interval of 4 weeks.

The invention is described more concretely with reference to the following Examples and Production Examples, which, however, are not intended to restrict the scope of the invention. In thin-layer chromatography in Examples and Production Examples, Silica gel6()F254 (Merck) was used for the plate, and a UV detector was used for detection.

WakogelTM C— 300 or C— 200(Wako Pure Chemical Industries) or NH (Fuji Silysia Chemical) was used for column silica gel. In MS spectrometry, used was JMS-SX102A (JEOL) or QUATTROII (Micromass). In NMR spectrometry, dimethylsulfoxide was used as the internal standard in a heavy dimethylsulfoxide solution; a spectrometer of Gemini-300 (300 MHz; Varian), VXR- 300 (300 MHz; Varian), Mercury 400 (400 MHz; Varian) or Inova 400(400 MHz; Varian) was used; and all δ values are by ppm.

The meanings of the abbreviations in NMR are mentioned below. s: singlet d: doublet dd: double doublet t: triplet dt: double triplet q: quartet m: multiplet br: broad

J: coupling constant Hz: hertz DMSO-d6: heavy dimethylsulfoxide

Production Example 1:

Production of 2-allyl-6-(methylthio)-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

1) Tert-butyl 1-allylhydrazinecarboxylate:

250 g of tert-butyl hydrazinecarboxylate was added to toluene (3 L) solution of 280 g of phthalic anhydride. Using a Dean-Stark water separator, the reaction mixture was heated under reflux for 3 hours. This was cooled to room temperature, the formed solid was taken out through filtration to obtain 516 g of crude tert-butyl (l,3-dioxo-l,3-dihydro-2H- isoindol-2-yl)carbamate.

520 g of potassium carbonate, 43.3 g of benzyltriethylammonium chloride and 250 mL of allyl bromide were added in that order to acetonitrile (3.5 L) solution of the above compound, and stirred at room temperature for 18 hours. 1.5 L of water was added to the reaction solution, and the acetonitrile layer was separated and concentrated. One L of water was added to the residue and the aqueous layer, extracted with ethyl acetate, and the ethyl acetate layer was washed with saturated saline water, and then dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the precipitated colorless solid was washed with hexane and dried to obtain 460 g of crude tert-butyl allyl(l,3-dioxo-l,3-dihydro-2H- isoindol-2-yl)carbamate. With cooling in an ice bath, 100 niL of methylhydrazine was added to tetrahydrofuran (3.0 L) solution of the above compound, then restored to room temperature, and stirred for 18 hours. The precipitated insoluble matter was taken out through filtration, and the filtrate was concentrated. A mixed solvent of hexane/ethyl acetate (3/1) was added to the residue, and the precipitated insoluble matter was taken out through filtration. This operation was repeated five times, then the filtrate was concentrated under reduced pressure, the resulting residue was distilled under reduced pressure to obtain 211 g of the entitled compound as a pale yellow oily substance. ESI-MS Found: m/z[M+H]+ 173.4. 2) Production of 2-allyl-6-(methylthio)-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one:

260 mL of N,N-diisopropylethylamine and 106 g of the hydrazine obtained in the above 1 were added to tetrahydrofuran (1.5 L) solution of 142 g of ethyl 4-chloro-2- (methylthio)pyridine-5-carboxylate, and stirred with heating under reflux for 18 hours. After cooled to room temperature, the reaction solution was evaporated under reduced pressure, and 500 mL of diethyl ether was added to the residue, and the precipitated solid was separated through filtration. The filtrate was evaporated under reduced pressure, the residue was cooled in an ice bath, 400 mL of trifluoroacetic acid was gradually added thereto, and stirred at room temperature for 1 hour and then at 70⁰C for 1 hour. The reaction solution was evaporated under reduced pressure, 500 mL of ethanol was added thereto and cooled in an ice bath, and 1.0 L of 6 N sodium hydroxide solution was added thereto and stirred at room temperature for 15 minutes. Cooled in an ice bath, the reaction solution was made acidic with 400 mL of concentrated hydrochloric acid, and then evaporated under reduced pressure. The residue was partitioned in chloroform and water, and the chloroform layer was extracted, washed with saturated saline water, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the formed yellow solid was taken out through filtration, washed with ethanol and diethyl ether, and dried to obtain 99.1 g of the entitled compound as a yellow solid. iH-NMR (400 MHz, DMSO-d6) δ: 8.66 (1.0H, brs), 5.83 (1.0H, ddt, J=17.1, 9.8, 5.4 Hz), 5.13

(1.0H, d, J=9.8 Hz), 5.06 (1.0H, d, J=17.1 Hz), 4.34 (2.0H, d, J=5.4 Hz), 2.51 (3.0H, s).

ESI-MS Found: m/z[M+H]+ 223.3.

Production Example 2:

Production of 6-rmethylthio)-l-phenyl-l,2-dihvdro-3H-pyrazolo[3.4-d]pyrimidin-3-one

60 mL of triethylamine was added to tetrahydrofuran (200 mL) solution of 25 g of ethyl 4-chloro-2-(methylthio)pyrimidine-5-carboxylate and 12.7 mL of phenylhydrazine, and stirred at room temperature for 18 hours. The solvent was concentrated under reduced pressure, water was added to the residue, then washed with ether, and made acidic with aqueous 5 N hydrochloric acid solution added thereto. The precipitated solid was taken out through filtration, and washed with water and 2-propanol to obtain 10.8 g of the entitled compound as a white solid. iH-NMR (400 MHz, CDCI3) δ: 12.18 (IH, s), 9.02 (IH, s), 8.13 (2H, dd, J=8.8, 1.0 Hz), 7.52

(2H, td, J=Il, 1.6 Hz), 7.26 (IH, tt, J=7.1, 1.0 Hz), 2.61 (3H, s).

ESI-MS Found: m/z[M+H]+ 259.1.

Example 1:

Production of 3-(2-allyl-6-{[4-(4-methylpiperazin-l-yl)phenyl]amino}-3-oxo-l,2-dihydro-3H- pyrazolor3,4-d1pyrimidin-l-ylVN,N-dimethylbenzamide

V) Production of methyl 3-[2-allyl-6-(methylthio)-3-oxo-l,2-dihydro-3H-pyrazolo[3,4- d]pyrimidin-l-yl]benzoate:

20 mL of pyridine was added to a chloroform solution of 7.5 g of 2-allyl-6- (methylthio)-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one, 6.1 g of copper(H) acetate and 10 g of [3-(methoxycarbonyl)]phenylboronic acid, and stirred at room temperature for 3 days. Aqueous 30 % ammonia solution and saturated saline water were added to the reaction liquid in that order, and extracted with chloroform. The organic layer was washed with saturated saline water, then dried with anhydrous magnesium sulfate, and the solvent was evaporated away. The crude product was purified through silica gel column chromatography (hexane/ethyl acetate) to obtain 6.7 g of methyl 3-[2-allyl-6-(methylthio)-3-oxo-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin- l-yl]benzoate as a yellow oily substance. iH-NMR (400 MHz, CDCI3) δ: 8.92 (IH, s), 8.11-8.06 (2H, m), 7.65-7.59 (2H, m), 5.68 (IH, ddd, J=YJX 10.2, 5.9 Hz), 5.13 (IH, dd, J=10.2, 1.0 Hz), 4.97 (IH, dd, J=17.1, 1.0 Hz), 4.45 (2H, d, J=5.9 Hz), 3.96 (3H, s), 2.51 (3H, s).

2) Production of methyl 3-[2-allyl-6-(methylsulfinyl)-3-oxo-l,2-dihydro-3H-pyrazolo[3,4- d]pyrimidin-l-yl]benzoate:

At 0⁰C, 6.5 g of m-chloroperbenzoic acid was added to a chloroform solution of 6.7 g of the compound obtained in the above reaction, and stirred for 30 minutes. Aqueous saturated sodium hydrogencarbonate solution was added to the reaction liquid, and extracted with chloroform/isopropanol (80/20). The organic layer was dried with anhydrous magnesium sulfate, and the solvent was evaporated away to obtain 5.6 g of crude methyl 3-[2-allyl-6- (methylsulfinyl)-3-oxo-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-l-yl]benzoate.

3) Production of methyl 3-(2-allyl-6-{[4-(4-methylpiperazin-l-yl)phenyl]amino}-3-oxo-l,2- dihydro-3H-pyrazolo[3,4-d]pyrimidin-l-yl]benzoate: 0.87 g of 4-(4-methyl-l-piperazinyl)aniline and 2 mL of N,N- diisopropylethylamine were added to a toluene solution of 1.7 g of the crude product obtained in the above reaction, and stirred at 70⁰C for 12 hours. The solvent was evaporated away, and the product was purified through silica gel column chromatography (chloroform/methanol) to obtain 2.2 g of methyl 3-(2-allyl-6-{[4-(4-methylpiperazin-l-yl)phenyl]amino}-3-oxo-l,2-dihydro-3H- pyrazolo[3,4-d]pyrimidin-l-yl]benzoate as a pale yellow solid. iH-NMR (400 MHz, CDCI3) δ: 8.81 (IH, s), 8.18-8.13 (IH, m), 8.04 (IH, d, J=7.8 Hz), 7.66-

7.56 (2H, m), 7.45 (2H, d, J=8.5 Hz), 6.88 (2H, d, J=8-.5 Hz), 5.68 (IH, ddd, J=17.1, 10.2, 6.3

Hz), 5.10 (IH, dd, J=10.2, 1.0 Hz), 4.98 (IH, dd, J=17.1, 1.0 Hz), 4.40 (2H, d, J=6.3 Hz), 3.97

(3H, s), 3.26-3.21 (4H, m), 2.72-2.64 (4H, m), 2.43 (3H, brs).

4) Production of 3-(2-allyl-6-{[4-(4-methylpiperazin-l-yl)phenyl]amino}-3-oxo-l,2-dihydro-3H- pyrazolo[3,4-d]pyrimidin-l-yl)-N,N-dimethylbenzamide:

Aqueous 1 N sodium hydroxide solution was added to a 1,4-dioxane/methanol (50/50) solution of 2.2 g of methyl 3-(2-allyl-6-{[4-(4-methylpiperazin-l-yl)phenyl]amino}-3- oxo-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-l-yl]benzoate, and stirred at room temperature for 2.5 hours. This was neutralized with 1 N hydrochloric acid, and the solvent was evaporated away to obtain a free carboxylic acid of the starting ester. To an N,N-dimethylformamide solution of the resulting carboxylic acid, added were 1.67 g of l-(3-dimethylaminopropyl)-3- ethylcarbodiimide hydrochloride, 1.18 g of 1-hydroxybenzotriazole, and 11 mL of 1.0 M dimethylamine/tetrahydrofuran solution, and stirred at room temperature for 6 hours. Aqueous saturated sodium hydrogencarbonate solution and water were added to the reaction liquid, extracted with chloroform/isopropanol (80/20), and purified through silica gel column chromatography (chloroform/methanol) to obtain 560 mg of 3-(2-allyl-6-{[4-(4-methylpiperazin- l-yl)phenyl] amino } -3 -oxo-1 ,2-dihydro-3H-pyrazolo [3 ,4-d]pyrimidin- 1 -yl)-N,N- dimethylbenzamide as a pale yellow solid. iH-NMR (400 MHz, CDCI3) δ: 8.81 (IH, s), 7.57-7.51 (2H, m), 7.49-7.38 (4H, m), 6.90 (2H, d,

J=8.8 Hz), 5.69 (IH, ddt, J=17.1, 10.2, 6.3 Hz), 5.10 (IH, dd, J=10.2, 1.0 Hz), 5.00 (IH, dd,

J=17.1, 1.0 Hz), 4.40 (2H, d, J=6.3 Hz), 3.32 (3H, s), 3.14 (3H, s), 2.99-2.92 (4H, m), 2.84-2.71

(4H, m), 2.50 (3H, s).

ESI-MS Found: m/z[M+H]+ 513.

Example 2:

Production of 2-allyl-6-{[3-rhydroxymethyl)-4-(4-methylpiperazin-l-yl)phenyl]amino}-l-r3- thienyl)-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

17.5 mg of the entitled compound was obtained as a yellow solid in the same manner as in Example 1-1 to 1-3, for which, however, 3-thienylboronic acid was used in place of [3-(methoxycarbonyl)]phenylboric acid used in Example 1-1, and [5-amino-2-(4- methylpiperazin-l-yl)phenyl]methanol was used in place of 4-(4-methylpiperazin-l-yl)aniline used in Example 1-3. iH-NMR (400 MHz, CDCI3) δ: 8.82 (IH, s), 7.17-7.63 (6H, m), 5.65-5.77 (IH, m), 5.13 (IH, d,

J=10.2 Hz), 5.04 (IH, d, J=17.1 Hz), 4.76 (2H, s), 4.42 (2H, d, J=6.3 Hz), 2.98-3.06 (4H, m),

2.50-2.76 (4H, m), 2.39 (3H, s).

ESI-MS Found: m/z[M+H]+ 478.

Example 3:

Production of 2-allyl-l-[3-(l-hydroxy-l-methylethyl)phenyl]-6-{[4-r4-methylpiperazin-l- yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

1) Production of 3-(l-hydroxy-l-methylethyl)phenylboronic acid:

In a nitrogen atmosphere with cooling with ice, 5.29 mL of 3'-bromoacetophenone was added to 25 mL of 2 M methylmagnesium iodide/diethyl ether solution and 100 mL of diethyl ether, and stirred for 20 minutes. Water and 2 N hydrochloric acid were added to the reaction liquid, extracted with ethyl acetate, washed with aqueous saturated sodium hydrogencarbonate solution and saturated saline water, and dried with anhydrous magnesium sulfate. The solvent was evaporated away under reduced pressure to obtain crude 2-(3- bromophenyl)propan-2-ol.

In a nitrogen atmosphere, 33 mL of 1.66 M n-butyllithium/hexane solution was dropwise added to tetrahydrofuran (200 mL) solution of the obtained compound at -6O⁰C or lower, and stirred for 20 minutes. 11.08 mL of triisopropoxyborane was added to the reaction liquid, and stirred for 30 minutes. Water was added to the reaction liquid, washed with diethyl ether, and the resulting aqueous layer was made acidic with aqueous 10 % phosphoric acid solution. This was extracted with ethyl acetate, washed with aqueous saturated sodium hydrogencarbonate solution and saturated saline water, and dried with anhydrous magnesium sulfate. The solvent was evaporated away under reduced pressure, and the resulting crystal was collected to obtain 3.13 g of the entitled compound as a white solid. iH-NMR (400 MHz, CDCI3) δ: 7.96 (2H, s), 7.88 (IH, brs), 7.60 (IH, d, J=7.3 Hz), 7.50 (IH, d,

J=8.3 Hz), 7.24 (IH, t, J=7.6 Hz), 4.93 (IH, s), 1.43 (6H, d, J=13.7 Hz).

2) Production of 2-allyl-l-[3-(l-hydroxy-l-methylethyl)phenyl]-6-{[4-(4-methylpiperazin-l- yl)phenyl] amino } - 1 ,2-dihydro-3H-pyrazolo [3 ,4-d]pyrimidin-3-one :

35.2 mg of the entitled compound was obtained as a yellow solid in the same manner as in Example 1-1 to 1-3, for which, however, the above boronic acid was used in place of [3-(methoxycarbonyl)]phenylboronic acid used in Example 1-1.

IH-NMR (400 MHz, CDCI3) δ: 8.80 (IH, s), 7.57 (IH, s), 7.47 (2H, d, J=4.9 Hz), 7.43 (2H, d,

J=8.8 Hz), 7.31-7.28 (IH, m), 6.88 (2H, d, J=8.8 Hz), 5.70 (IH, ddt, J=17.1, 10.0, 6.3 Hz), 5.10 (IH, dd, J=10.0, 1.2 Hz), 4.98 (IH, dd, J=17.1, 1.5 Hz), 4.38 (2H, d, J=6.3 Hz), 3.21 (4H, t, J=4.1 Hz), 2.66 (4H, s), 2.41 (3H, s), 1.62 (6H, s). ESI-MS Found: m/z[M+H]+ 500.

Example 4:

Production of 2-allyl-l-[3-(dimethylaminomethyl)phenyl]-6-{[4-(4-methylpiperazm-l- yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

1) Production of 2-allyl-l-[3-(dimethylaminomethyl)phenyl]-6-(methylthio)-l,2-dihydro-3H- pyrazolo[3,4-d]pyrimidin-3-one:

2.9 mL of methanesulfonyl chloride and 11 mL of N,N-diisopropylethylamine were added in that order to chloroform (50 mL) solution of 3.0 g of 2-allyl-l-[3- (hydroxymethyl)phenyl]-6-(methylthio)-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one that had been obtained by the use of [3-(hydroxymethyl)phenyl]boronic acid in place of [3- (methoxycarbonyl)]phenylboronic acid used in Example 1-1, and stirred at room temperature for 1 hour. The reaction liquid was washed with 0.5 N hydrochloric acid, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain crude 2-allyl- l-[3-(methylsulfonyloxymethyl)phenyl]-6-(methylthio)-l,2-dihydro-3H-pyrazolo[3,4- d]pyrimidin-3-one as a yellow oily substance.

20 mL of 2 M dimethylamine/tetrahydrofuran solution was added to tetrahydrofuran (100 mL) solution of 1.5 g of the above compound, and stirred at room temperature for 18 hours. The solvent was evaporated away under reduced pressure, and the residue was separated and purified through silica gel column chromatography (ethyl acetate) to obtain 2.5 g of the entitled compound as a yellow solid. iH-NMR (400 MHz, CDCI3) δ: 8.90 (IH, s), 7.53-7.26 (4H, m), 5.73-5.62 (IH, m), 5.11 (IH, dd,

J=10.2, 1.0 Hz), 4.95 (IH, dd, 3=17.1, 1.0 Hz), 4.44 (2H, d, J=3.7 Hz), 3.49 (2H, s), 2.48 (3H, s),

2.27 (6H, s).

ESI-MS Found: m/z M+H]+356.1.

2) Production of 2-allyl-l-[3-(dimethylaminomethyl)phenyl]-6-{[4-(4-methylpiperazin-l- yl)phenyl] amino }- 1 ,2-dihydro-3H-pyrazolo [3 ,4-d]pyrimidin-3 -one :

4 N hydrochloric acid/ethyl acetate solution was added to 100 mg of the compound obtained in the above 1, stirred at room temperature, and the solvent was evaporated away under reduced pressure to obtain 2-allyl-l-[3-(dimethylaminomethyl)phenyl]-6- (methylthio)-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one hydrochloride.

70 mg of m-chloroperbenzoic acid was added to N,N-dimethylformamide (2 mL) solution of the above compound, and stirred at room temperature for 15 minutes. The reaction liquid was washed with aqueous saturated sodium hydrogencarbonate solution, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain crude 2-allyl-l-[3-(dimethylaminomethyl)phenyl]-6-(methylsulfinyl)-l,2-dihydro-3H- pyrazolo[3,4-d]pyrimidin-3-one as a white solid. 50 nig of 4-(4-methylpiperazin-l-yl)aniline and 0.1 mL of N,N- diisopropylethylamine were added in that order to dimethylsulfoxide/toluene (1/10, 10 mL) solution of the above compound, and stirred at 120°C for 15 hours. The solvent was evaporated away under reduced pressure, water was added thereto, and extracted with ethyl acetate and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the residue was separated and purified through basic silica gel column chromatography (entyl acetate) to obtain 11.4 mg f the entitled compound as a yellow solid. iH-NMR (400 MHz, CDCI3) δ: 8.80 (IH, s), 7.48-7.33 (6H, m), 6.87 (2H, d, J=8.8 Hz), 5.80-

5.60 (IH, m), 5.09 (IH, dd, J=10.2, 1.0 Hz), 4.97 (IH, dd, J=17.1, 1.5 Hz), 4.38 (IH, d, J=5.9

Hz), 3.51 (2H, s), 3.18 (4H, t, J=4.9 Hz), 2.60 (4H, t, J=4.9 Hz), 2.37 (3H, s), 2.28 (6H, s).

ESI-MS Found: m/z[M+H]+ 499.

Example 5:

Production of 2-allyl-6-{[3-hydroxymethyl-4-(4-methylpiperazin-l-yl)phenyl]amino}-l-pyridin-

2-yl-l,2-dihvdro-3H-pyrazolo[3,4-dlpyrimidin-3-one

1) Production of 2-allyl-6-(methylthio)-l-pyridin-2-yl-3H-pyrazolo[3,4-d]pyrimidin-3-one:

2.4 mL of N,N'-dimethylethylenediamine was added to 1,4-dioxane (50 mL) solution of 4.44 g of 2-allyl-6-(methylthio)-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one, 3,80 g of copper(I) iodide, 5.33 g of 2-iodopyridine and 3.80 g of potassium carbonate, and stirred overnight at 95°C. The reaction liquid was cooled, aqueous ammonia was added thereto and extracted with ethyl acetate, washed with saturated saline water and dried with anhydrous magnesium sulfate. The solvent was evaporated away under reduced pressure, and crystallized with ethyl acetate to obtain 5.15 g of the entitled compound as a white solid. iH-NMR (400 MHz, CDCI3) δ: 8.94 (IH, s), 8.52 (IH, d, J=5.1 Hz), 7.90 (2H, d, J=3.5 Hz),

7.29-7.25 (IH, m), 5.68 (IH, ddt, J=17.0, 10.2, 6.3 Hz), 5.05 (IH, d, J=10.2 Hz), 4.91 (IH, d, J=17.0 Hz), 4.85 (IH, d, J=6.3 Hz), 2.58 (3H, s). ESI-MS Found: m/z[M+H]+ 300.

2) Production of 2-allyl-6-{[3-hydroxymethyl-4-(4-methylpiperazin-l-yl)phenyl]amino}-l- pyridin-2-yl-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one:

796 mg of m-chloroperbenzoic acid (> 65 %) was added to toluene (20 mL) solution of 898 mg of 2-allyl-6-(methylthio)-l-pyridin-2-yl-3H-pyrazolo[3,4-d]pyrimidin-3-one, and stirred for 30 minutes. 1.60 mL of N,N-diisopropylethylamine, 800 mg of [5-amino-2-(4- methylpiperazin-l-yl)phenyl]methanol and 10 mL of tetrahydrofuran were added to the reaction liquid, and stirred overnight. Aqueous saturated sodium hydrogencarbonate solution was added to the reaction liquid, and extracted with a mixed solution of chloroform/isopropanol (80/20). This was dried with anhydrous magnesium sulfate, the solvent was evaporated away, and the residue was purified through basic silica gel column chromatography (hexane/ethyl acetate = 50/50 to 0/100). The resulting crystal was recrystallized from ethanol to obtain 941 mg of the entitled compound as a white crystal. iH-NMR (400 MHz, CDCI3) δ: 8.84 (IH, s), 8.53 (IH, d, J=4.8 Hz), 7.91 (IH, dd, 7.88 (IH, dd,

J=8.8, 7.6 Hz), 7.87 (IH, d, J=7.6 Hz), 7.64 (IH, s), 7.33 (IH, d, J=8.8 Hz), 7.26 (IH, dd, J=8.8,

4.8 Hz), 7.19 (IH, d, J=8.8 Hz), 5.68 (IH, ddd, J=17.2, 10.4, 5.6 Hz), 5.50 (IH, s), 5.01 (IH, d,

10.4 Hz), 4.91 (IH, d, J=17.2 Hz), 4.79 (2H, s), 4.79 (2H, d, J=5.6 Hz), 3.01 (4H, m), 2.62 (4H, m), 2.37 (3H, s).

ESI-MS Found: m/z[M+H]+ 472.

Example 6:

Production of 2-allyl-l-(6-aminopyridin-2-yl)-6-{ [3-methyl-4-(4-methylpiperazin-l- yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

1) Production of di-tert-butyl {6-[2-allyl-6-(methylthio)-3-oxo-l,2-dihydro-3H-pyrazolo[3,4- d]pyrimidin-l-yl]-2-pyridinyl}imidedicarboxylate:

2.00 g of the entitled compound was obtained as a white solid in the same manner as in Example 5-1, for which, however, di-tert-butyl (6-bromopyridin-2-yl)imidedicarboxylate was sued in place of 2-iodopyridine used in Example 5-1. iH-NMR (400 MHz, CDCI3) δ: 8.92 (IH, s), 7.92 (IH, t, J=8.0 Hz), 7.80 (IH, d, J=8.8 Hz), 7.35

(IH, d, J=7.8 Hz), 5.63 (IH, ddt, J=17.1, 10.2, 6.3 Hz), 5.03 (IH, dd, J=10.2, 1.0 Hz), 5.00 (IH, dd, J=17.1, 1.2 Hz), 4.82 (2H, d, J=6.3 Hz), 2.58 (3H, s), 1.51 (18H, s). ESI-MS Found: m/z[M+H]+ 515.

2) Production of 2-allyl-l-(6-aminopyridin-2-yl)-6-{[3-methyl-4-(4-methylpiperazin-l- yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

53 mg of m-chloroperbenzoic acid (> 65 %) was added to toluene (2 mL) solution of 103 mg of di-tert-butyl {6-[2-allyl-6-(methylthio)-3-oxo-2,3-dihydro-lH-pyrazolo[3,4- d]pyrimidin-l-yl]-2-pyridinyl}imidedicarboxylate, and stirred for 30 minutes. 0.105 mL of N,N- diisopropylethylamine and 49 mg of 3-methyl-4-(4-methylpiperazm-l-yi)aniline were added to the reaction liquid, and stirred overnight. Aqueous saturated sodium hydrogencarbonate solution was added to the reaction liquid, ethyl acetate was added thereto for extraction, the resulting extract was washed with saturated saline water, and dried with anhydrous magnesium sulfate. The solvent was evaporated away, and the residue was purified through basic silica gel column chromatography (hexane/ethyl acetate = 1/1 to 0/1). After concentrated, 93.2 mg of a white solid was obtained. 2 niL of trifluoroacetic acid was added to the obtained compound, stirred, and saturated sodium hydrogencarbonate was added thereto, extracted with ethyl acetate, washed with saline water, and dried with anhydrous magnesium sulfate. The solvent was evaporated away under reduced pressure to obtain 51.8 mg of the entitled compound as a white solid. IH-NMR (400 MHz, CDCI3) δ: 8.81 (IH, s), 7.60 (IH, t, J=7.8 Hz), 7.52 (IH, s), 7.34 (IH, dd,

J=8.8, 2.4 Hz), 7.00 (IH, d, J=8.3 Hz), 6.43 (IH, d, J=7.8 Hz), 5.71 (IH, ddt, J=16.8, 10.2, 5.9

Hz), 5.06 (IH, dd, J=10.2, 1.0 Hz), 5.00 (IH, dd, J=16.8, 1.2 Hz), 4.71 (2H, d, J=5.9 Hz), 4.58

(2H, s), 2.95 (4H, t, J=4.6 Hz), 2.66 (4H, s), 2.42 (3H, s), 2.31 (3H, s).

ESI-MS Found: m/z[M+H]+ 412.

Example 7:

Production of 2-allyl-l-(6-aminopyridin-2-yl)-6-{[4-(4-methylpiperazin-l-vDphenyl]amino}-l,2- dihvdro-3H-pyrazolo[3,4-d]pyrimidin-3-one

966 mg of the entitled compound was obtained as a yellow solid in the same manner as in Example 6-1 to 6-2, for which, however, 4-(4-methylpiperazin-l-yl)aniline was used in place of 3-methyl-4-(4-methylpiperazin-l-yl)aniline used in Example 6-2. iH-NMR (400 MHz, CDCI3) δ: 8.80 (IH, s), 7.59 (IH, t, J=7.8 Hz), 7.39 (IH, brs), 6.91 (2H, d,

J=8.8 Hz), 6.42 (IH, d, J=8.3 Hz), 5.71 (IH, ddt, J=17.1, 10.2, 5.9 Hz), 5.06 (IH, dd, J=10.2, 1.0

Hz), 5.00 (IH, dd, J=17.1, 1.0 Hz), 4.70 (2H, d, J=5.9 Hz), 4.57 (2H, s), 3.20 (4H, t, J=5.1 Hz),

2.61 (4H, t, J=4.9 Hz), 2.38 (3H, s).

ESI-MS Found: m/z[M+H]+ 458.

Example 8:

Production of 2-allyl-l-{6-[(dimethylamino)methyl]pyridin-2-yl}-6-{ [4-(4-methylpiperazin-l- yl)phenyl]amino}-l,2-dihvdro-3H-pyrazolo[3,4-d]pyrimidin-3-one

1) Production of 2-allyl-l-[6-(hydroxymethyl)-2-pyridinyl]-6-(methylthio)-l,2-dihydro-3H- pyrazolo [3 ,4-d]pyrimidin-3-one :

3.40 g of the entitled compound was obtained as a white solid in the same manner as in Example 5-1, for which, however, (6-bromopyridin-2-yl)methanol was used in place of 2- iodopyridine used in Example 5-1. iH-NMR (400 MHz, CDCI3) δ: 8.94 (IH, s), 7.91 (IH, t, J=7.8 Hz), 7.78 (IH, dd, J=8.0, 0.7 Hz),

7.27 (IH, d, J=7.8 Hz), 5.76-5.66 (IH, m), 5.07 (IH, dd, J=10.2, 1.0 Hz), 4.95 (IH, dd, J=17.1, 1.0 Hz), 4.84-4.77 (4H, m), 2.58 (3H, s). ESI-MS Found: m/z[M+H]+ 330.

2) Production of 2-allyl-l-{6-[(dimethylamino)methyl]-2-pyridinyl}-6-(methylthio)-l,2-dihydro- 3H-pyrazolo[3,4-d]pyrimidin-3-one hydrochloride:

1.16 mL of triethylamine and 0.451 mL of methanesulfonyl chloride were added to tetrahydrofuran (20 mL) solution of 1.37 g of the compound obtained in the above 1, and stirred for 30 minutes, and then 6 mL of 2.0 M dimethylamine/tetrahydrofuran solution was added to the reaction liquid and stirred for 8 hours. Water was added to the reaction liquid, and extracted with ethyl acetate. This was washed with saturated saline water, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure. 10 mL of ethyl acetate and 1.5 mL of 4 N hydrochloric acid-dioxane solution were added to the resulting residue, then the solvent was concentrated under reduced pressure, and the residue was crystallized with methanol/diethyl ether to obtain 1.50 g of the entitled compound as a white solid. iH-NMR (400 MHz, DMSO-d6) δ: 8.17 (IH, s), 7.36 (IH, t, J=7.8 Hz), 7.21 (IH, d, J=7.8 Hz),

6.76 (IH, d, J=7.3 Hz), 4.92 (IH, ddt, J=17.1, 10.2, 6.0 Hz), 4.26 (IH, dd, 3=10.2, 1.5 Hz), 4.14

(IH, dd, 1=17.1, 1.5 Hz), 4.00 (2H, dt, J=6.0, 1.3 Hz), 3.75 (2H, s), 2.14 (6H, s), 1.78(3H, s).

ESI-MS Found: m/z[M+H]+ 357.

3) Production of 2-allyl-l-{6-[(dimethylamino)methyl]pyridin-2-yl}-6-{[4-(4-methylpiperazin-l- yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one:

65 mg of m-chloroperbenzoic acid was added to N,N-dimethylformamide (2 mL) solution of 100 mg of the compound obtained in the above 2, and stirred at room temperature for 15 minutes. The reaction liquid was washed with aqueous saturated sodium hydrogencarbonate solution, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain crude 2-allyl-l-{6-[(dimethylamino)methyl]pyridin-2-yl}-6- (methylsulfinyl)-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one as a white solid.

40 mg of 4-(4-methylpiperazin-l-yl)aniline and 0.1 mL of N,N- diisopropylethylamine were added in that order to dimethylsulfoxide/toluene (1/10, 10 mL) solution of 40 mg of the above compound, and stirred at 120⁰C for 15 hours. The solvent was evaporated away under reduced pressure, water was added thereto, extracted with ethyl acetate, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the residue was separated and purified through basic silica gel column chromatography (ethyl acetate) to obtain 8.4 mg of the entitled compound as a yellow solid. iH-NMR (400 MHz, CDCI3) δ: 8.82 (IH, s), 7.82 (IH, t, J=7.8 Hz), 7.74 (IH, d, J=7.8 Hz), 7.47

(2H, d, J=8.8 Hz), 7.39 (IH, d, J=7.3 Hz), 6.92 (2H, d, J=6.3 Hz), 5.74-5.63 (IH, m), 5.00 (IH, dd, 3=10.2, 1.0 Hz), 4.89 (IH, dd, J=17.1, 1.0 Hz), 4.80 (2H, d, J=5.9 Hz), 3.64 (2H, s), 3.22 (4H, t, J=4.9 Hz), 2.64 (4H, d, J=4.4 Hz), 2.39 (3H, s), 2.34 (6H, s).

ESI-MS Found: m/z[M+H]+ 500.

Example 9:

Production of 2-allyl-l-[6-(l-hydroxy-l-methylethyl)pyridin-2-yl]-6-{[4-(4-methylpiperazin-l- vflphenvπaminoM,2-dihvdro-3H-pyrazolor3,4-d1pvrimidin-3-one

1) Production of 2-(6-bromo-2-pyridinyl)-2-propanol:

In a nitrogen atmosphere, 30 mL of 3 M methylmagnesium iodide/diethyl ether was added to 300 mL of diethyl ether solution of 8.72 g of methyl 6-bromopyridine-2- carboxylate. Water and 2 N hydrochloric acid were added to the reaction liquid, and extracted with ethyl acetate. This was washed with aqueous saturated sodium hydrogencarbonate solution and saturated saline water, and dried with anhydrous magnesium sulfate. The solvent was evaporated away under reduced pressure to obtain 8.51 g of crude 2-(6-bromo-2-pyridinyl)-2- propanol as a yellow oily substance. iH-NMR (400 MHz, CDC13) δ: 7.56 (IH, t, J=7.8 Hz), 7.38 (IH, dd, J=7.8, 1.0 Hz), 7.36 (IH, dd, J=7.8, 1.0 Hz), 1.55(6H, s). ESI-MS Found: m/z[M+H]+ 216, 218.

2) Production of 2-allyl-l-[6-(l-hydroxy-l-methylethyl)-2-pyridinyl]-6-(methylthio)-l,2-dihydro- 3H-pyrazolo[3,4-d]pyrimidin-3-one:

12.89 g of the entitled compound was obtained in the same manner as in Example 5-1, for which, however, the compound obtained in the above reaction was used in place of 2- iodopyridine used in Example 5-1. iH-NMR (400 MHz, CDCI3) δ: 8.95 (IH, s), 7.91 (IH, t, J=8.0 Hz), 7.76 (IH, d, J=7.3 Hz), 7.40

(IH, dd, J=7.8, 1.0 Hz), 5.70 (IH, ddt, J=17.1, 10.2, 6.3 Hz), 5.06 (IH, dd, J=10.2, 1.0 Hz), 4.93 (IH, dd, J=17.1, 1.2 Hz), 4.81 (2H, d, J=6.3 Hz), 2.59 (4H, s), 1.59 (6H, s). ESI-MS Found: m/z[M+H]+ :358.

3) Production of 2-allyl-l-[6-(l-hydroxy-l-methylethyl)pyridin-2-yl]-6-{[4-(4-methylpiperazin- l-yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one:

817 mg of m-chloroperbenzoic acid (> 65 %) was added to toluene (20 mL) solution of 1.10 g of the above produce, and stirred fro 20 minutes. 1.61 mL of N₅N- diisopropylethylamine and 706 mg of 4-(4-methylpiperazin-l-yl)aniline were added to the reaction liquid, and stirred overnight. Aqueous saturated sodium hydrogencarbonate solution was added to the reaction liquid, extracted with ethyl acetate, washed with saturated saline water, and dried with anhydrous magnesium sulfate. The solvent was evaporated away, and the residue was purified through basic silica gel column chromatography (hexane/ethyl acetate = 1/1 to 0/1, ethyl acetate/ethanol = 98/2). After concentrated, this was recrystallized from ethyl acetate to obtain 1.20 g of the entitled compound as a yellow solid. iH-NMR (400 MHz, CDCI3) δ: 8.83 (IH, s), 7.86 (IH, dd, J=8.0, 7.8 Hz), 7.75 (IH, d, J=7.3

Hz), 7.49 (IH, brs), 7.48 (2H, d, J=9.0 Hz), 7.34 (IH, d, J=7.4 Hz), 6.93 (2H, d, J=9.0 Hz), 5.70

(IH, ddt, J=17.2, 10.0, 6.5 Hz), 5.04 (IH, d, J=10.0 Hz), 4.94 (IH, d, J=17.2 Hz), 4.74 (2H, d,

J=6.5 Hz), 3.26 (4H, t, J=4.8 Hz), 2.73 (4H, brs), 2.44 (3H, s), 1.59 (6H, s).

ESI-MS Found: m/z[M+H]+ 501.

Example 10:

Production of 2-allyl-6-{[4-(4-ethylpiperazin-l-yl)phenyl]amino}-l-[6-(l-hydroxy-l- methylethyl)pyridin-2-yl]-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

50.3 mg of the entitled compound was obtained as a yellow solid in the same manner as in Example 9-1 to 9-3, for which, however, 4-(4-ethyl-l-piperazinyl)aniline was used in place of 4-(4-methylpiperazin-l-yl)aniline used in Example 9-3. iH-NMR (400 MHz, CDCI3) δ: 8.83 (IH, s), 7.85 (IH, t, J=7.8 Hz), 7.76 (IH, d, J=7.8 Hz), 7.46

(2H, d, J=8.8 Hz), 7.34 (IH, d, J=8.3 Hz), 6.93 (2H, d, J=8.8 Hz), 5.76-5.64 (IH, m), 5.04 (IH, dd, J=10.2, 1.0 Hz), 4.94 (IH₅ dd, J=17.1, 1.0 Hz), 4.75 (2H, d, J=6.3 Hz), 4.00 (IH, brs), 3.23

(4H, t, J=4.9 Hz), 2.65 (4H, t, J=4.9 Hz), 2.51 (2H, q, J=7.3 Hz), 1.59 (6H, s), 1.16 (3H, t, J=7.3

Hz).

ESI-MS Found: m/z[M+H]+ 515.

Example 11:

Production of 6- { [4-(4-acetylpiperazin-l -yl)phenyl] amino} -2-allyl- 1 - [6-(l-hydroxy- 1 - methylethyl)pyridin-2-yl]-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

66.4 mg of the entitled compound was obtained as a yellow solid in the same manner as in Example 9-1 to 9-3, for which, however, 4-(4-acetyl-l-piperazinyl)aniline was used in place of 4-(4-methylpiperazin-l-yl)aniline used in Example 9-3. iH-NMR (400 MHz, CDCI3) δ: 8.84 (IH, s), 7.87 (IH, t, J=7.8 Hz), 7.74 (IH, d, J=8.8 Hz), 7.50

(2H, d, J=8.8 Hz), 7.36 (IH, d, J=8.3 Hz), 6.94 (2H, d, J=8.8 Hz), 5.76-5.65 (IH, m), 5.04 (IH, d,

J=10.2 Hz), 4.94 (IH, d, J=17.1 Hz), 4.74 (2H, d, J=5.9 Hz), 4.03-3.95 (IH, m), 3.80 (2H, t,

J=4.9 Hz), 3.65 (2H, t, J=5.1 Hz), 3.17 (2H, t, J=4.9 Hz), 3.14 (2H, t, J=5.1 Hz), 2.16 (3H, s),

1.59 (6H, s).

ESI-MS Found: m/z[M+H]+ 529.

Example 12:

Production of 2-allyl-6-({4-[4-(2-hydroxyethyl)piperazin-l-yl]phenyl}amino)-l-[6-(l-hydroxy-l- methylethyl)pyridin-2-yl]-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

40 mg of the entitled compound was obtained as a yellow solid in the same manner as in Example 9-1 to 9-3, for which, however, 2-[4-(4-aminophenyl)-l- piperazinyl]ethanol was used in place of 4-(4-methylpiperazin-l-yl)aniline used in Example 9-3. IH-NMR (400 MHz, CDCI3) δ: 8.83 (IH, s), 7.86 (IH, t, J=7.8 Hz), 7.75 (IH, d, J=7.8 Hz), 7.47

(2H, d, J=8.8 Hz), 7.34 (IH, d, J=8.3 Hz), 6.93 (2H, d, J=8.8 Hz), 5.76-5.65 (IH, m), 5.04 (IH, d, J=10.2 Hz), 4.94 (IH, d, J=17.1 Hz), 4.74 (2H, d, J=6.3 Hz), 4.03-3.95 (IH, m), 3.69 (2H, t,

J=5.1 Hz), 3.22 (4H, t, J=4.9 Hz), 2.73 (4H, t, J=4.6 Hz), 2.65 (2H, t, J=5.4 Hz), 1.59 (6H, s).

ESI-MS Found: m/z[M+H]+ 531.

Example 13:

Production of 2-allyl-l-[6-(l-hydroxycyclobutyl)pyridin-2-yl]-6-{ [4-(4-methyrpiperazin-l- yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

1) Production of l-(6-bromo-2-pyrimidinyl)cyclobutanol:

In a nitrogen atmosphere at -1O⁰C, 10.8 mL of 2.66 M n-butyllithium/hexane solution was dropwise added to 16 mL of 0.9 M n-butylmagnesium chloride/tetrahydrofuran solution, and toluene (60 mL) solution of 9.48 g of 2,6-dibromopyridine was dropwise added thereto at O⁰C or lower. The reaction liquid was stirred for 1.5 hours, then cooled in a dry ice/acetone bath, and 5.0 g of cyclobutanone was added thereto at -50⁰C or lower. After stirred for 10 minutes, water and 2 N hydrochloric acid were added to the reaction liquid, and the organic layer was separated, washed with aqueous saturated sodium hydrogencarbonate solution and saturated saline water, and then dried with anhydrous magnesium sulfate. After concentrated under reduced pressure, the residue was purified through silica gel column chromatography (hexane/ethyl acetate = 20/1 to 4/1) to obtain 5.30 g of the entitled compound as a yellow oily substance. iH-NMR (400 MHz, CDCI3) δ: 7.60 (IH, t, J=7.8 Hz), 7.52 (IH, dd, J=7.8, 1.0 Hz), 7.40 (IH, dd, J=7.8, 1.0 Hz), 2.53-2.48 (4H, m), 2.12-2.01 (IH, m), 1.91-1.82 (IH, m). ESI-MS Found: m/z[M+H]+ 228, 230.

2) Production of 2-allyl-l-[6-(l-hydroxycyclobutyl)-2-pyridinyl]-6-(methylthio)-l,2-dihydro-3H- pyrazolo [3,4-d]pyrimidin-3 -one :

1.44 g of the entitled compound was obtained in the same manner as in Example 9-2, for which, however, the compound obtained in the above reaction was used in place of 2-(6- bromo-2-pyridinyl)-2-propanol used in Example 9-2. iH-NMR (400 MHz, CDCI3) δ: 8.94 (IH, s), 7.95 (IH, t, J=8.0 Hz), 7.77 (IH, d, J=7.8 Hz), 7.54

(IH, d, J=7.8 Hz), 5.70 (IH, ddt, J=17.1, 10.2, 6.3 Hz), 5.07 (IH, d, J=10.2 Hz), 4.94 (IH, d, J=17.1 Hz), 4.80 (2H, d, J=6.3 Hz), 2.58 (3H, s), 2.56-2.50 (4H, m), 2.15-2.03 (IH, m), 1.97- 1.84 (IH, m). ESI-MS Found: m/z[M+H]+ 370.

3) Production of 2-allyl-l-[6-(l-hydroxycyclobutyl)pyridin-2-yl]-6-{[4-(4-methylpiperazin-l- yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one:

80.8 mg of the entitled compound was obtained as a yellow solid in the same manner as in Example 9-3, for which, however, the compound obtained in the above reaction was used in place of 2-allyl-l-[6-(l-hydroxy-l-methylethyl)-2-pyridinyl]-6-(methylthio)-l,2- dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one used in Example 9-3. iH-NMR (400 MHz, CDCI3) δ: 8.83 (IH, s), 7.90 (IH, t, J=7.8 Hz), 7.77 (IH, d, J=7.8 Hz), 7.48

(2H, dd, J=12.2, 8.3 Hz), 7.48 (IH, brs), 6.93 (2H, d, J=9.3 Hz), 5.70 (IH, tdd, J=5.9, 17.1, 10.0

Hz), 5.04 (IH, dd, J=ICO, 1.2 Hz), 4.94 (IH, dd, J=17.1, 1.0 Hz), 4.73 (2H, d, J=5.9 Hz), 4.20

(IH, s), 3.24 (4H, t, J=4.6 Hz), 2.65 (4H, brs), 2.53 (4H, t, J=8.0 Hz), 2.41 (3H, s), 2.14-2.06 (IH, m), 1.96-1.84 (IH, m).

ESI-MS Found: m/z[M+H]+ 513.

Example 14:

Production of 2-allyl-l-[6-(2-hydroxy-2-methylpropyl)pyridin-2-yl]-6-{[4-(4-methylpiperazin-l- yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

1) Production of l-(6-bromopyridin-2-yl)-2-methylpropan-2-ol:

In a nitrogen atmosphere, 400 mL of tetrahydrofuran containing 31 mL of diisopropylamine was cooled in a dry ice/acetone bath, and 82.7 mL of 2.66 M n- butyllithium/hexane solution was added thereto, and 50 mL of tetrahydrofuran containing 34.4 g of 6-bromopicoline was dropwise added thereto at -7O⁰C or lower. After the addition, 29.4 mL of acetone was added thereto at -6O⁰C or lower. After stirred for 35 minutes, water was added to the reaction liquid, and the organic solvent was concentrated under reduced pressure. This was extracted with diethyl ether, washed with saturated saline water, and dried with anhydrous magnesium sulfate. After concentrated under reduced pressure, the residue was purified through distillation to obtain 27.60 g of the entitled compound as a colorless oily substance. iH-NMR (400 MHz, CDCI3) δ: 7.50 (IH, t, J=7.6 Hz), 7.37 (IH, d, J=7.8 Hz), 7.12 (IH, d,

J=7.8 Hz), 2.91 (2H, s), 1.23 (6H, s). ESI-MS Found: m/z[M+H]+ :230, 232.

2) Production of 2-allyl-l-[6-(2-hydroxy-2-methylpropyl)pyridin-2-yl]-6-(methylthio)-l,2- dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one:

20.70 g of the entitled compound was obtained in the same manner as in Example 9-2, for which, however, the compound obtained in the above reaction was used in place of 2-(6- bromo-2-pyridinyl)-2-propanol used in Example 9-2. IH-NMR (400 MHz, CDCI3) δ: 8.93 (IH, s), 7.84 (IH, t, J=7.8 Hz), 7.71 (IH, d, J=8.3 Hz), 7.15

(IH, d, J=7.3 Hz), 5.67 (IH, ddt, J=16.8, 10.2, 6.3 Hz), 5.05 (IH, dd, J=10.2, 1.0 Hz), 4.93 (IH, dd, J=16.8, 1.2 Hz), 4.77 (2H, d, J=6.3 Hz), 2.97 (2H, s), 2.58 (3H, s), 1.25 (6H, s). ESI-MS Found: m/z[M+H]+ 372.

3) Production of 2-allyl-l-[6-(2-hydroxy-2-methylpropyl)pyridin-2-yl]-6-{[4-(4-methylpiperazin- l-yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

1.06 g of the entitled compound was obtained as a yellow solid in the same manner as in Example 9-3, for which, however, the compound obtained in the above reaction was used in place of 2-allyl-l-[6-(l-hydroxy-l-methylethyl)-2-pyridinyl]-6-(methylthio)-l,2- dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one used in Example 9-3. iH-NMR (400 MHz, CDCI3) δ: 8.82 (IH, s), 7.79 (IH, t, J=7.8 Hz), 7.66 (IH, brs), 7.45 (2H₅ d,

J=8.8 Hz), 7.08 (IH, d, J=7.8 Hz), 6.93 (2H, d, J=8.8 Hz), 5.78-5.62 (IH, m), 5.13-4.94 (2H, m),

4.63 (2H, s), 3.23 (4H, t, J=4.6 Hz), 2.98 (2H, s), 2.64 (4H, s), 2.40 (3H, s), 1.24 (6H, s).

ESI-MS Found: m/z[M+H]+ 515.

Example 15:

Production of 2-allyl-l-[6-(2-hydroxy-2-methylpropyl)pyridin-2-yl]-6-{[4-(l-methylpiperidin-4- yl)phenyl]amino}-l,2-dmydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

36.8 mg of the entitled compound was obtained as a yellow solid in the same manner as in Example 14-1 to 14-3, for which, however, 4-(l-methylpiperidin-4-yl)aniline was used in place of 4-(4-methylpiperazin-l-yl)aniline used in Example 14-3. lH-NMR (400 MHz, CDCI3) δ: 8.85 (IH, s), 7.89-7.76 (2H, brm), 7.80 (IH, t, J=7.8 Hz), 7.52

(2H, d, J=8.3 Hz), 7.22 (2H, d, J=8.3 Hz), 7.10 (IH, d, J=7.8 Hz), 5.77-5.64 (IH, brm), 5.08 (IH, d, J=9.8 Hz), 5.01 (IH, d, J=17.6 Hz), 4.71-4.58 (2H, brm), 3.05 (2H, d, 3=11.2 Hz), 2.99 (2H, s),

2.56-2.45 (IH, m), 2.38 (3H, s), 2.21-2.07 (2H, m), 1.95-1.81 (4H, m), 1.24 (6H, s).

ESI-MS Found: m/z[M+H]+ 514.

Example 16:

Production of 2-allyl-l-[6-(2-hvdroxy-lΛ,2-trimethylpropyπpyridin-2-yll-6-f[4-(4- methylpiperazin-l-yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

1) Production of ethyl 2-(6-bromopyridin-2-yl)-2-methylpropionate:

In a nitrogen atmosphere, 100 mL of tetrahydrofuran containing 14 mL of diisopropylamine was cooled in a dry ice-acetone bath, and 38 mL of 2.66 M n- butyllithium/hexane solution was added thereto to prepare lithium-diisopropylamide. This was dropwise added to 100 mL of tetrahydrofuran containing 4.55 mL of 6-bromopicoline and 6.06 mL of diethyl carbonate, at -6O⁰C or lower. After stirred for 20 minutes, 6.23 mL of methyl iodide was added thereto and heated up to room temperature. Water was added to the reaction liquid, extracted with diethyl ether, washed with saturated saline water, and dried with anhydrous magnesium sulfate. After concentrated under reduced pressure, the residue was purified through silica gel column chromatography (hexane/ethyl acetate = 100/0 to 8/1) to obtain 10.72 g of the entitled compound as a colorless oily substance. lH-NMR (400 MHz, CDCI3) δ: 7.49 (IH, t, J=7.8 Hz), 7.33 (IH, dd, J=7.8, 1.0 Hz), 7.22 (IH, dd, J=7.8, 1.0 Hz), 4.16 (2H, q, J=7.0 Hz), 1.59 (6H, s), 1.20 (3H, t, J=7.1 Hz), 0.00 (IH, d,

J=3.4 Hz).

ESI-MS Found: m/z[M+H]+ 272, 274.

2) Production of 3-(6-bromopyridin-2-yl)-2,3-dimethylbutan-2-ol:

In a nitrogen atmosphere, 13 mL of 2 M methylmagnesium iodide/diethyl ether solution was added to diethyl ether (20 mL) solution of 2.72 g of ethyl 2-(6-bromopyridin-2-yl)- 2-methylpropionate with cooling in an ice bath. The reaction liquid was stirred at room temperature for 3 hours, and then water and aqueous 10 % phosphoric acid solution were added thereto, extracted with diethyl ether, washed with aqueous saturated sodium hydrogencarbonate solution and saturated saline water, and then dried with anhydrous magnesium sulfate. After concentrated under reduced pressure, the residue was purified through silica gel column chromatography (hexane/ethyl acetate = 9/1 to 8/1) to obtain 1.47 g of the entitled compound as a colorless oily substance. iH-NMR (400 MHz, CDC13) δ: 7.53 (IH, t, J=7.8 Hz), 7.35 (IH, d, J=7.3 Hz), 7.31 (IH, d,

J=7.8 Hz), 1.38 (6H, s), 1.09 (6H, s).

ESI-MS Found: m/z[M+H]+ 258, 260.

3) Production of 2-allyl-l-[6-(2-hydroxy-l,l,2-trimethylpropyl)pyridin-2-yl]-6-{[4-(4- methylpiperazin-l-yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one:

74.5 mg of the entitled compound was obtained as a yellow solid in the same manner as in Example 9-2 to 9-3, for which, however, the compound obtained in the above reaction was used in place of 2-(6-bromo-2-pyridyl)-2-propanol used in Example 9-2. iH-NMR (400 MHz, CDCI3) δ: 8.82 (IH, s), 7.81 (IH, t, J=7.9 Hz), 7.81 (IH, brs), 7.45 (2H, d,

J=8.4 Hz), 7.30 (IH, s), 6.93 (2H, d, J=9.2 Hz), 5.71 (IH, s), 5.08 (2H, s), 4.63 (2H, s), 3.24 (4H, s), 2.66 (4H, s), 2.41 (3H, s), 1.47 (6H, s), 1.09 (6H, s).

ESI-MS Found: m/z[M+H]+ 543.

Example 17:

Production of 2-allyl-6-{[4-(4-methylpiperazin-l-yl)phenyl]amino}-l-[6-r2-oxopyrrolidin-l- yl)pyridin-2-yl]-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

With cooling with ice, 0.012 mL of triethylamine and 12.4 mg of 4-chlorobutyric acid chloride were added to tetrahydrofuran (1 mL) solution of 20 mg of the compound obtained in Example 7, 2-allyl-l-(6-aminopyridin-2-yl)-6-{[4-(4-methylpiperazin-l-yl)phenyl]amino}-l,2- dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one, and stirred at room temperature for 1 hour. Water was added to the reaction mixture, extracted with chloroform, and the organic layer was washed with saturated saline water, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, the resulting residue was dissolved in 1 mL of N,N- dimethylformamide, and 5 mg of potassium tert-butoxide was added thereto and stirred at room temperature for 30 minutes. Saturated ammonium chloride solution was added to the reaction mixture, extracted with ethyl acetate, and the organic layer was washed with saturated saline water and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through preparative thin-layer chromatography (chloroform/methanol = 10/1) to obtain 5 mg of the entitled compound as a yellow solid. iH-NMR (400 MHz, CDCI3) δ: 8.82 (IH, s), 8.34 (IH, d, J=8.0 Hz), 7.85 (IH, t, J=8.0 Hz), 7.58

(IH, d, J=8.0 Hz), 7.49-7.34 (IH, brm), 7.46 (2H, d, J=8.8 Hz), 6.92 (2H, d, J=8.8 Hz), 5.68 (IH, ddt, J=17.1, 10.2, 5.9 Hz), 5.04 (IH, dd, J=10.2, 1.0 Hz), 4.94 (IH, dd, J=17.1. 1.0 Hz), 4.76 (2H, d, J=5.9 Hz), 4.13-4.04 (2H, m), 3.30-3.20 (4H, m), 2.76-2.61 (6H, m), 2.42 (3H, s), 2.21-2.09

(2H, m).

ESI-MS Found: m/z[M+H]+ 526.

Example 18:

Production of N-{[6-(2-allyl-6-{[4-(4-methylpiperazin-l-yl)phenyl]amino}-3-oxo-l,2-dihydro-

3H-pyrazolo[3,4-d]pyrimidin-l-yl)pyridin-2-yl]methyl}-N-methylmethanesulfonamide

1) Production of 2-allyl-l-[6-(hydroxymethyl)pyridin-2-yl]-6-{[4-(4-methylpiperazin-l- yl)phenyl] amino } - 1 ,2-dihydro-3H-pyrazolo [3 ,4-d]pyrimidin-3 -one :

1.36 g of imidazole and 1.81 g of tert-butyl(chloro)dimethylsilane were added to N,N-dimethylformamide (30 mL) solution of 3.29 g of the compound obtained in Example 8-1, and stirred overnight. Water was added to the reaction liquid, and extracted with diethyl ether. This was washed with saturated saline water, and dried with anhydrous magnesium sulfate. After concentrated under reduced pressure, the resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate = 9/1 to 4/1), and the solvent was evaporated away under reduced pressure. 40 mL of toluene and 3.20 g of m-chloroperbenzoic acid (> 65 %) were added to the residue, and stirred for 30 minutes. 5.20 mL of N,N-diisopropylethylarnine and 2.29 g of 4-(4-methylpiperazin-l-yl)aniline were added to the reaction liquid, and stirred overnight. Aqueous saturated sodium hydrogencarbonate solution was added to the reaction liquid, and extracted with ethyl acetate. This was dried with anhydrous magnesium sulfate, the solvent was evaporated away, the residue was purified through silica gel column chromatography (chloroform/ethanol = 100/1 to 100/3), and the solvent was evaporated away under reduced pressure. 50 mL of 4 N hydrochloric acid was added to the residue, and stirred, and then the solution was made alkaline with aqueous 4 N sodium hydroxide solution. This was extracted with a mixed solution of chloroform/isopropanol (80/20), dried with anhydrous magnesium sulfate, the solvent was evaporated away, and the residue was crystallized in ethyl acetate to obtain 3.78 g of the entitled compound as a yellow crystal. iH-NMR (400 MHz, CDCI3) δ: 8.83 (IH, s), 7.86 (IH, t, J=6.0 Hz), 7.75 (IH, d, J=8.2 Hz), 7.46

(2H, d, J=8.6 Hz), 7.40 (IH, brs), 7.22 (IH, d, J=7.6 Hz), 6.92 (2H, d, J=9.0 Hz), 5.71 (IH, ddt, J=16.8, 10.2, 5.9 Hz), 5.06 (IH, d, J=10.2 Hz), 4.96 (IH, d, J=16.8 Hz), 4.81 (2H, d, J=5.5 Hz), 4.71 (IH, d, J=5.9 Hz), 3.23 (4H, brs), 3.14 (IH, t, J=5.5 Hz), 2.64 (4H, brs), 2.40 (3H, s). ESI-MS Found: m/z[M+H]+ 473.

2) Production of 2-allyl-l-{6-[(methylamino)methyl]pyridin-2-yl}-6-{[4-(4-methylpiperazin-l- yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one:

4.46 mL of triethylamine and 1.0 mL of methanesulfonyl chloride were added to tetrahydrofuran (120 mL) solution of 3.78 g of the compound obtained in the above 1, and stirred. 20 mL of 2.0 M methylamine/tetrahydrofuran solution was added to the reaction liquid, and stirred overnight. Water was added to the reaction liquid, and extracted with ethyl acetate. This was washed with saturated saline water, dried with anhydrous magnesium sulfate, concentrated under reduced pressure, and the resulting residue was purified through basic silica gel column chromatography (hexane/ethyl acetate = 50/50 to 0/100 to chloroform) to obtain 3.38 g of the entitled compound as a yellow solid. iH-NMR (400 MHz, CDCI3) δ: 8.82 (IH, s), 7.81 (IH, t, J=7.8 Hz), 7.72 (IH, d, J=7.8 Hz), 7.46

(2H, d, J=8.8 Hz), 7.25 (IH, d, J=7.3 Hz), 6.92 (2H, d, J=9.3 Hz), 5.69 (IH, ddt, J=17.1, 10.2, 6.3 Hz), 5.02 (IH, dd, J=10.2, 1.5 Hz), 4.92 (IH, dd, J=17.1, 1.5 Hz), 4.75 (2H, d, J=6.3 Hz), 3.91 (2H, s), 3.21 (4H, t, J=4.9 Hz), 2.62 (4H, t, J=4.9 Hz), 2.51 (3H, s), 2.38 (3H, s). ESI-MS Found: m/z[M+H]+ 486.

3) Production of N-{[6-(2-allyl-6-{[4-(4-methylpiperazin-l-yl)phenyl]amino}-3-oxo-l,2- dihydro-3H-pyrazolo[3,4-d]pyrimidin-l-yl)pyridin-2-yl]methyl}-N-methylmethanesulfonamide: 1.50 mL of triethylamine and 0.4 mL of methanesulfonyl chloride were added to tetrahydrofuran (50 mL) solution of 1.70 g of the compound obtained in the above 2, and stirred. Water was added to the reaction liquid, and extracted with ethyl acetate. This was washed with saturated saline water, dried with anhydrous magnesium sulfate, concentrated under reduced pressure, and the resulting residue was crystallized from 15 mL of ethyl acetate and 10 mL of ethanol to obtain 849 mg of the entitled compound as a yellow solid. iH-NMR (400 MHz, CDCI3) δ: 8.83 (IH, s), 7.89 (IH, t, J=7.8 Hz), 7.81 (IH, d, J=8.3 Hz), 7.48

(IH, d, J=9.3 Hz), 7.47 (IH, brs), 7.41 (2H, d, J=7.3 Hz), 6.93 (2H, d, J=8.8 Hz), 5.68 (IH, ddt,

J=17.1, 10.2, 6.3 Hz), 5.03 (IH, d, J=10.2 Hz), 4.92 (IH, d, J=18.0 Hz), 4.75 (2H, d, J=6.3 Hz),

4.50 (2H, s), 3.38 (4H, brs), 2.95 (3H, s), 2.92 (4H, brs), 2.91 (3H, s), 2.58 (3H, s).

ESI-MS Found: m/z[M+H]+ 564.

Example 19:

Production of 2-allyl- 1 - [6-(2-hydroxy- 1 , 1 -dimethylethyl)pyridin-2-yl] - 6- { [4-(4-methylpiperazin- l-yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

1) Production of 2-(6-bromopyridm-2-yl)-2-methylpropan-l-ol:

In a dry ice/acetone bath, 100 mL of a toluene solution of 1.01 M diisobutylaluminium hydride was added to toluene (50 mL) solution of 10.72 g of the compound obtained in Example 16-1, heated up to room temperature, and stirred for 40 minutes. With cooling with ice, aqueous saturated ammonium chloride solution was added to the reaction liquid, and the organic layer was separated. This was washed with aqueous saturated sodium hydrogencarbonate solution and saturated saline water, dried with anhydrous magnesium sulfate, concentrated under reduced pressure, and the residue was purified through silica gel column chromatography (ethyl acetate) to obtain 8.74 g of the entitled compound as a colorless oily substance. iH-NMR (400 MHz, CDCI3) δ: 7.52 (IH, t, J=7.8 Hz), 7.33 (IH₅ dd, J=7.8, 1.0 Hz), 7.27 (IH, d,

J=7.8 Hz), 3.74 (2H, s), 1.32 (6H, s). ESI-MS Found: m/z[M+H]+ 230, 232.

2) Production of 2-allyl-l-[6-(2-hydroxy-l,l-dimethylethyl)pyridin-2-yl]-6-(methylthio)-l,2- dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one:

7.45 g of the entitled compound was obtained in the same manner as in Example 9-2, for which, however, the compound obtained in the above reaction was used in place of 2-(6- bromo-2-pyridinyl)-2-propanol used in Example 9-2. iH-NMR (400 MHz, CDCI3) δ: 8.93 (IH, s), 7.86 (IH, t, J=8.0 Hz), 7.60 (IH, d, J=8.8 Hz), 7.31

(IH, d, J=7.8 Hz), 5.67 (IH, ddt, 1=17.1, 10.2, 6.3 Hz), 5.05 (IH, dd, J=10.2, 1.0 Hz), 4.92 (IH, dd, J=17.1, 1.5 Hz), 4.79 (2H, d, J=6.3 Hz), 3.78 (2H, s), 2.58 (3H, s), 1.37 (6H, s). ESI-MS Found: m/z[M+H]+ 372.

3) Production of 2-allyl-l-[6-(2-hydroxy-l,l-dimethylethyl)pyridin-2-yl]-6-{[4-(4- methylpiperazin- 1 -yl)phenyl] amino } - 1 ,2-dihydro-3H-pyrazolo [3 ,4-d]pyrimidin-3 -one :

1.4 g of the entitled compound was obtained as a yellow solid in the same manner as in Example 9-3, for which, however, the compound obtained in the above reaction was used in place of 2-allyl-l-[6-(l-hydroxy-l-methylethyl)-2-pyridinyl]-6-(methylthio)-l,2-dihydro-3H- pyrazolo[3,4-d]pyrimidin-3-one used in Example 9-3. iH-NMR (400 MHz, CDCI3) δ: 8.83 (IH, s), 7.81 (IH, t, J=7.8 Hz), 7.52-7.41 (3H, m), 7.25

(IH, d, J=9.3 Hz), 6.92 (2H, dd, J=6.8, 2.4 Hz), 5.72 (IH, brs), 5.14-4.96 (2H, brm), 4.64 (2H, brs), 3.79 (2H, d, J=6.3 Hz), 3.24 (4H, t, J=5.0 Hz), 2.65 (4H, brs), 2.41 (3H, s), 1.38 (6H, s).

ESI-MS Found: m/z[M+H]+ 515.

Example 20:

Production of l-[6-(l -hydroxy- 1 -methylethyl)pyridm-2- yl] -6- { [4-(4-methyrpiperazin- 1 - yl)phenvnamino|-2-(2-propynylVl,2-dihvdro-3H-pyrazolor3,4-dlpyrimidin-3-one

1) Production of l-[6-(l-hydroxy-l-methylethyl)pyridin-2-yl]-6-(methylthio)-2-(2-propynyl)-l,2- dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one:

440 mg of ammonium formate and 230 mg of [1,1'- bis(diphenylphosphino)ferrocene]palladium(π) dichloride were added to tetrahydrofuran (13.6 mL) solution of 500 mg of 2-allyl-l-[6-(l-hydroxy-l-methylethyl)-2-pyridinyl]-6-(methylthio)- l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one produced in Example 9, and stirred at 90⁰C for 3 hours. The reaction liquid was cooled to room temperature, distilled water was added thereof, and extracted with a mixed solution of chloroform/isopropanol (80/20). This was dried with anhydrous sodium sulfate, and the solvent was evaporated away under reduced pressure to obtain 770 mg of a black amorphous substance. 61.0 mg of sodium hydride was added to N,N- dimethylformamide (14.0 mL) solution of the resulting compound, and stirred for 30 minutes. 0.316 mL of propargyl bromide was added to the reaction solution, and stirred for 3.5 hours. Aqueous saturated sodium hydrogencarbonate solution and saturated saline water were added to the reaction liquid, and extracted with a mixed solution of chloroform/isopropanol (80/20). This was dried with anhydrous sodium sulfate, and the solvent was evaporated away under reduced pressure to obtain a black amorphous substance. The resulting amorphous substance was purified through silica gel column chromatography (hexane/ethyl acetate) to obtain 254 mg of the entitled compound as a white compound. iH-NMR (400 MHz, CDCI3) δ: 8.94 (IH, s), 7.94 (2H, d, J=3.6 Hz), 7.43 (IH, t, J=3.6 Hz), 4.97

(2H, d, J=2.4 Hz), 2.62 (3H, s), 2.16 (IH, t, J=2.4 Hz), 1.59 (6H, s).

ESI-MS Found: m/z[M+H]+ 357.

2) Production of l-[6-(l-hydroxy-l-methylethyl)pyridin-2-yl]-6-{[4-(4-methylpiperazin-l- yl)phenyl]amino}-2-(2-propynyl)-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one:

7.3 mg of the entitled compound was obtained as a yellow solid in the same manner as in Example 9-3, for which, however, the compound obtained in the above reaction was used in place of 2-allyl-l-[6-(l-hydroxy-l-methylethyl)-2-pyridinyl]-6-(methylthio)-l,2- dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one used in Example 9-3. iH-NMR (400 MHz, CDCI3) δ: 8.83 (IH, s), 7.92 (IH, d, J=8.0 Hz), 7.87 (IH, dd, J=8.0, 8.0

Hz), 7.47 (2H, d, J=7.6 Hz), 7.35 (IH, d, J=8.0 Hz), 6.94 (2H, d, J=7.6 Hz), 4.89 (2H, d, J=2.0

Hz), 3.23 (4H, m), 2.63 (4H, m), 2.39 (3H, s), 2.13 (IH, t, J=2.0 Hz), 1.59 (6H, s).

ESI-MS Found: m/z[M+H]+ 499.

Example 21:

Production of 2-allyl-l-[6-(3-methyl-2-oxoimidazolidin-l-yl)pyridin-2-yl]-6-{[4-(4- methylpiperazin-l-yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one

1) Production of 2-allyl-l-(6-bromopyridin-2-yl)-6-(methylthio)-l,2-dihydro-3H-pyrazolo[3,4- d]pyrimidin-3-one:

In the same manner as in Example 5-1, but using 2,6-dibromopyridin in place of 2-iodopyridin used in Example 5-1, 2.94 g of the entitled compound was obtained as a white solid. lH-NMR(400MHz,CDCl3) d:8.94(lH_Js),7.95(lH,d,J=7.8Hz),7.73(lH,t,J=8.0Hz),7.43(lH,d,J=7.8Hz),5.69(lH,ddt,J=17.1,10

.2,6.3Hz),5.06(lH,dd,J=10.2,1.2Hz),5.00(lH,d,J=17.1Hz),4.88(2H,d,J=6.3Hz),2.60(3H,s).

2) Production of 2-allyl-l-[6-(3-methyl-2-oxoimidazolidin-l-yl)pyridin-2-yl]-6-(methylthio)-l,2- dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one: l-methylimidazolidin-2-one (96 mg), copper iodide (76 mg), potassium carbonate (110 mg) and N,N'-dimethylethane-l,2-diamine (85 μL) were added to a dioxane solution (5 mL) of 2-allyl-l-(6-bromopyridin-2-yl)-6-(methylthio)-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3- one (150 mg), and stirred overnight in a sealed tube under heat at 100⁰C.

The reaction liquid was cooled, aqueous ammonia solution was added to it, and extracted three times with chloroform. The organic layer was washed with saturated saline water, dried with anhydrous magnesium sulfate, filtered, and the solvent was evaporated away. The obtained crude product was purified through silica gel column chromatography to obtain 136.4 mg of the entitled compound as a white solid. IH-NMR (400 MHz, CDCI3) d: 8.92 (IH, s), 8.26 (IH, d, J=8.4 Hz), 7.81 (IH, dd, J=8.4, 7.6

Hz), 7.41 (IH, d, J=7.6 Hz), 5.66 (IH, ddd, J=16.8, 10.0, 6.4 Hz), 5.06 (IH, d, J=10.0 Hz), 4.95 (IH, d, J=16.8 Hz), 4.80 (2H, d, J=6.4 Hz), 4.01 (2H, t, J=8.0 Hz), 3.51 (IH, t, J=8.0 Hz), 2.94 (3H, s), 2.57 (3H, s). ESI-MS Found: m/z[M+H]398.

3) Production of 2-allyl-l-[6-(3-methyl-2-oxoimidazolidin-l-yl)pyridin-2-yl]-6-{[4-(4- methylpiperazin-l-yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one:

In the same manner as in Example 5-2, but using 4-(4-methylpiperazin-l- yl)aniline in place of [5-amino-2-(4-methylpiperazin-l-yl)phenyl]methanol used in Example 5-2 and using 2-allyl-l-[6-(3-methyl-2-oxoimidazolidin-l-yl)pyridin-2-yl]-6-(methylthio)-l,2- dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one in place of 2-allyl-6-(methylthio)-l-pyridin-2-yl-3H- pyrazolo[3,4-d]pyrimidin-3-one, 115.6 mg of the entitled compound was obtained as a yellow solid. iH-NMR (400 MHz, CDCI3) d: 8.81 (IH, s), 8.22 (IH, d, J=8.4 Hz), 7.78 (IH, dd, J=8.4, 8.0

Hz), 7.46 (2H, d, J=8.0 Hz), 7.40 (IH, d, J=8.0 Hz), 6.90 (2H, d, J=8.0 Hz), 5.68 (IH, ddd,

J=16.8, 10.4, 6.0 Hz), 5.04 (IH, d, J=10.4 Hz), 4.95 (IH, d, J=16.8 Hz), 4.74 (2H, d, J=6.0 Hz),

4.02 (2H, t, J=8.4 Hz), 3.49 (2H, t, J=8.4 Hz), 3.02 (4H, m), 2.94 (3H, S), 2.60 (4H, m), 2.37 (3H, s).

ESI-MS Found: m/z[M+H]541.

Industrial Applicability

The compounds of the invention have excellent Weel kinase-inhibitory effect and are therefore useful in the field of medicines, especially treatment of various cancers.

Claims

1. A compound of a general formula (I):

wherein,

Al is selected from the following formula (aal):

RIC is a hydrogen atom, a lower alkenyl group or a group of -Q3-A3(Rld)Rle;

Rid and Rle are independently a hydrogen atom, a halogen atom, a cyano group, a hydroxyl group, a lower alkyl group or a hydroxy-lower alkyl group, or together form a lower alkylene group wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom, a sulfur atom, a sulfinyl group, a sulfonyl group, a carbonyl group, a vinylene group or a group of -N(RIf)-, and/or substituted by a hydroxyl group or a lower alkyl group;

Rl is a lower alkenyl group or a lower alkynyl group;

R2 is a phenyl, pyridyl or thienyl group, which may have a group of -Q4- A4(Rlg)Rlh_;

Q4 is a single bond or a lower alkylene group, wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom or a carbonyl group, and/or substituted by a lower alkyl group; Rig and Rlh are independently a hydrogen atom, a halogen atom, a cyano group, a hydroxyl group, a lower alkyl group, a lower alkoxy-lower alky! group, a lower alkanoyl group, a lower alkoxycarbonyl group or a lower alkylsulfonyl group, or together form a lower alkylene group, wherein one or two or more methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom, a sulfur atom, a sulfinyl group, a sulfonyl group, a carbonyl group or a group of -N(Rli)-, and/or substituted by a halogen atom or a lower alkyl group;

Rli is a hydrogen atom, a lower alkyl group or a halo-lower alkyl group;

R5 and R6 are independently a hydrogen atom, a lower alkyl group or a hydroxy- lower alkyl group, or a salt thereof.

2. The compound as claimed in claim 1, or a salt thereof, wherein Rl is a lower alkenyl group.

3. The compound as claimed in claim 2, or a salt thereof, wherein Rl is an allyl group.

4. The compound as claimed in claim 1, or a salt thereof, wherein R2 is a phenyl or pyridyl group having a group of -Q4-A4(Rlg)Rlh.

5. The compound as claimed in claim 1, or a salt thereof, wherein Rl c is a hydrogen atom or a group of -Q3-A3(Rld)Rle, and in the group of -Q3-A3(Rld)Rle_;

(ii) A3 is a methine group optionally substituted by a hydroxyl group or a lower alkyl group, Q3 is a lower alkylene group wherein one or two methylene groups constituting the lower alkylene group may be independently replaced by an oxygen atom, a carbonyl group or a sulfonyl group, and/or substituted by a hydroxyl group, and Rid and Rle are independently a hydrogen atom, a halogen atom, a cyano group or a lower alkyl group.

6. The compound as claimed in claim 1, or a salt thereof, which is as follows: 3-(2-allyl-6-{[4-(4-methylpiperazin-l-yl)phenyl]amino}-3-oxo-l,2-dihydro-3H- pyrazolo[3,4-d]pyrimidin-l-yl)-N,N-dimethylbenzamide,

2-allyl-l-[3-(l-hydroxy-l-methylethyl)phenyl]-6-{[4-(4-methylpiperazin-l- yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one, 2-allyl-l-[3-(dimethylaminomethyl)phenyl]-6-{[4-(4-methylpiperazin-l- yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

2-allyl-6- { [3 -hydroxymethyl-4-(4-methylpiperazin- 1 -yl)phenyl] amino } - 1 -pyridin- 2-yl-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

2-allyl-l-(6-aminopyridin-2-yl)-6-[{4-(4-methylpiperazin-l-yl)phenyl]amino}- l,2-dihydro-3H-pyrazolo [3 ,4-d]pyrimidin-3 -one,

2-allyl-l-[6-(l-hydroxy-l-methylethyl)pyridin-2-yl]-6-{[4-(4-methylpiperazin-l- yl)phenyl]amino}-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

6-{[4-(4-acetylpiperazin-l-yl)phenyl]amino}-2-allyl-l-[6-(l-hydroxy-l- methylethyl)pyridin-2-yl]-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

2-allyl-6-({4-[4-(2-hydroxyethyl)piperazin-l-yl]phenyl}ammo)-l-[6-(l-liydroxy- l-methylethyl)pyridm-2-yl]-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one,

N-{ [6-(2-allyl-6- { [4-(4-methylpiperazin- 1 -yl)phenyl] amino } -3 -oxo- 1 ,2-dihydro- 3H-pyrazolo[3,4-d]pyrimidin-l-yl)pyridin-2-yl]methyl}-N-methylmethanesulfonamide, or l-[6-(l-hydroxy-l-methylethyl)pyridin-2-yl]-6-{[4-(4-methylpiperazin-l- yl)phenyl]amino}-2-(2-propynyl)-l,2-dihydro-3H-pyrazolo[3,4-d]pyrimidm-3-one.

7. A pharmaceutical composition comprising a therapeutically-effective amount of the compound as claimed in claim 1, or a salt thereof, and pharmaceutically acceptable carrier or diluent.

8. An anticancer agent comprising the pharmaceutical composition of claim

7.

9. A combined preparation for simultaneous, separate, or sequential administration in the treatment of cancer, comprising following two separate preparations (a) and

(b):

(a) a preparation comprising, together with a pharmaceutically acceptable carrier or diluent, the compound of above formula (I) or a pharmaceutically acceptable salt thereof; and

(b) a preparation comprising, together with a pharmaceutically acceptable carrier or diluent, one anticancer agent selected from the group consisting of anticancer alkylating agents, anticancer antimetabolites, anticancer antibiotics, plant-derived anticancer agents, anticancer platinum-coordinatedcomplex compounds, anticancer camptothecin derivatives, anticancer tyrosine kinase inhibitors, monoclonal antibodies, interferons, biological response modifiers, and other anticancer agents or a pharmaceutically acceptable salt thereof, wherein: the anticancer alkylating agents are nitrogen mustard N-oxide, cyclophosphamide, ifosfamide, melphalan, busulfan, mitobronitol, carboquone, thiotepa, ranimustine, nimustine, temozolomide, and carmustine; the anticancer antimetabolites are methotrexate, 6-mercaptopurine riboside, mercaptopurine, 5-fluorouracil, tegafur, doxifluridine, carmofur, cytarabine, cytarabine ocfosfate, enocitabine, S-I, gemcitabine, fludarabine, and pemetrexed disodium; the anticancer antibiotics are actinomycin D, doxorubicin, daunorubicin, neocarzinostatin, bleomycin, peplomycin, mitomycin C, aclarubicin, pirarubicin, epirubicin, zinostatin stimalamer, idarubicin, sirolimus, and valrubicin; the plant-derived anticancer agents are vincristine, vinblastine, vindeshine, etoposide, sobuzoxane, docetaxel, paclitaxel, and vinorelbine; the anticancer platinum-coordinatedcomplex compounds are cisplatin, carboplatin, nedaplatin, and oxaliplatin; the anticancer camptothecin derivatives are irinotecan, topotecan, and camptothecin; the anticancer tyrosine kinase inhibitors are gefitinib, imatinib, and erlotinib; the monoclonal antibodies are cetuximab, bevacizumab, rituximab, alemtuzumab, and trastuzumab; the interferons are interferon α, interferon α-2a, interferon α-2b, interferon β, interferon γ-la, and interferon γ-nl, the biological response modifiers are krestin, lentinan, sizofiran, picibanil, or ubenimex, and the other anticancer agents are mitoxantrone, L-asparaginase, procarbazine, dacarbazine, hydroxycarbamide, pentostatin, tretinoin, alefacept, darbepoetin alfa, anastrozole, exemestane, bicalutamide, leuprorelin, flutamide, fulvestrant, pegaptanib octasodium, denileukin diftitox, aldesleukin, thyrotropin alfa, arsenic trioxide, bortezomib, capecitabine, and goserelin.

10. A pharmaceutical composition comprising, together with a pharmaceutically acceptable carrier or diluent, the compound according to Claim 1, or a pharmaceutically acceptable salt thereof; and an anticancer agent selected from the group consisting of anticancer alkylating agents, anticancer antimetabolites, anticancer antibiotics, plant-derived anticancer agents, anticancer platinum-coordinatedcomplex compounds, anticancer camptothecin derivatives, anticancer tyrosine kinase inhibitors, monoclonal antibodies, biological response modifiers, and other anticancer agents, wherein the definition of each anticancer agent is the same as defined in Claim 9, or a pharmaceutically acceptable salt thereof.

11. A radiation sensitizer comprising the pharmaceutical composition as claimed in claim 7.

12. A sensitizer for an anticancer agent comprising the pharmaceutical composition as claimed in claim 7, wherein the anticancer agent is selected from the group consisting of anticancer alkylating agents, anticancer antimetabolites, anticancer antibiotics, plant-derived anticancer agents, anticancer platinum-coordinatedcomplex compounds, anticancer camptothecin derivatives, anticancer tyrosine kinase inhibitors, monoclonal antibodies, biological response modifiers, and other anticancer agents, wherein the definition of each anticancer agent is the same as defined in Claim 9, or a pharmaceutically acceptable salt thereof.

13. Use of the compound as claimed in claim 1 or a salt thereof for manufacturing an anticancer agent.