(S)-5-Methyl-tetrahydropyran-2-one 1 is a by-product in the production of key intermediates of steroidal hormones. Asymmetric synthesis of natural oxacyclododecindione-type macrolactones 2 and 3 has been realized for the first time from (S)-1 in seven and eight steps with 37% and 27% overall yield, respectively.
( S )-5-Methyl-tetrahydropyran-2-one 1是生产甾体激素关键中间体的副产品。首次从 ( S ) -1分 7 步和 8 步实现了天然氧杂环十二烷二酮型大环内酯2和3的不对称合成,总收率分别为 37% 和 27%。
PROCESSES OF PREPARING A JAK1 INHIBITOR AND NEW FORMS THERETO
申请人:Incyte Corporation
公开号:US20150344497A1
公开(公告)日:2015-12-03
This invention relates to processes for preparing a JAK1 inhibitor having Formula Ia:
as well as new forms of the inhibitor.
这项发明涉及制备具有Ia式的JAK1抑制剂的过程,以及该抑制剂的新形式。
(METH)ACRYLATE COMPOUND, (METH)ACRYLIC COPOLYMER AND PHOTOSENSITIVE RESIN COMPOSITION CONTAINING SAME
申请人:MITSUBISHI GAS CHEMICAL COMPANY, INC.
公开号:US20160347896A1
公开(公告)日:2016-12-01
The present invention provides a resist or a compound for use as a resist, which is highly sensitive and well-balanced without losing the fundamental physical properties required as a chemically amplified resist (e.g., resolution, line edge roughness (LER)).
The present invention is directed to a (meth)acrylate compound represented by general formula (1) and a process for preparation thereof, as well as a (meth)acrylic copolymer obtainable by polymerization of the (meth)acrylate compound of general formula (1) and a photosensitive resin composition thereof:
(wherein R
1
represents a hydrogen atom or a methyl group, R
2
represents a linear or branched alkyl group containing 2 to 4 carbon atoms, and each R
3
may be the same or different and represents a group represented by the following formula (2) or (3), etc.)
(provided that formulae (2) and (3) are as defined in the specification of the present application).
9-MEMBERED FUSED RING DERIVATIVE
申请人:Shionogi & Co., Ltd.
公开号:US20180079727A1
公开(公告)日:2018-03-22
The purpose of the present invention is to provide novel compounds having ACC2 selective inhibitory activity. In addition, the present invention provides a pharmaceutical composition comprising the compound.
A compound of Formula:
or its pharmaceutically acceptable salt,
wherein, R
1
is substituted or unsubstituted fused aromatic heterocyclyl represented by Formula:
wherein,
ring B is 5-membered ring, ring C is 6-membered ring;
ring A is substituted or unsubstituted non-aromatic carbocycle or the like;
-L
1
- is —O—(CR
6
R
7
)m- or the like;
-L
2
- is —O—(CR
6
R
7
)n- or the like;
each R
6
is independently hydrogen or the like;
each R
7
is independently hydrogen or the like;
each m is independently an integer of 0, 1, 2 or 3;
each n is independently an integer of 1, 2 or 3;
R
2
is substituted or unsubstituted alkyl;
R
3
is hydrogen or substituted or unsubstituted alkyl;
R
4
is substituted or unsubstituted alkylcarbonyl or the like.