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Title:
7H−ピロロ[2,3−d]ピリミジン誘導体の製造方法及びその合成中間体
Document Type and Number:
Japanese Patent JP6434678
Kind Code:
B2
Abstract:
The present invention provides processes for preparing 7H-pyrrolo[2,3-d]pyrimidine derivatives, which are useful as a Janus kinase (JAK) inhibitor, intermediates thereof, and processes for preparing the intermediates. The present invention provides processes for preparing 3-[(3S,4R)-3-methyl-6-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1,6-diazaspiro[3.4]octan-1-yl]-3-oxopropanenitrile using salts of (3S,4R)-1-benzyl-3-methyl-1,6-diazaspiro[3.4]octane with organic acids.

Inventors:
Dream Takiguchi
Akinobu Azuma
Takayuki Inaba
Takashi Watanabe
Bamboo city wing
Anas Kraskow Petersen
Pair Veze
Kim Rebek Jensen
Jan Bornholt
Selenium epdorp
Application Number:
JP2018518551A
Publication Date:
December 05, 2018
Filing Date:
December 20, 2017
Export Citation:
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Assignee:
Japan Tobacco Inc.
Leo Pharma Actiesl Scab
International Classes:
C07D519/00; C07C271/22; C07D205/08; C07D403/06; C07D487/10; C07D491/107
Foreign References:
WO2011013785A1
Other References:
MAJER, Zsuzsanna et al.,Spirobis[2-pyrrolidinones]. II. Synthesis and absolute configuration of 1,7-diazaspiro[4,4]nonane-2,,Collection of Czechoslovak Chemical Communications,1982年,Vol.47, No.3,pp.950-960,ISSN:0366-547X, DOI:10.1135/cccc19820950
Attorney, Agent or Firm:
Norihito Yamao
Nagatoshi Shinagawa
Kure Hidenori