| CPC C07D 403/04 (2013.01) [A01N 43/54 (2013.01); A01N 43/56 (2013.01); A01N 43/58 (2013.01); A01N 43/80 (2013.01); A01N 43/90 (2013.01); C07D 207/325 (2013.01); C07D 207/337 (2013.01); C07D 207/34 (2013.01); C07D 401/04 (2013.01); C07D 401/14 (2013.01); C07D 409/14 (2013.01); C07D 413/04 (2013.01); C07D 471/04 (2013.01); C07D 487/04 (2013.01)] | 9 Claims |
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1. A method, comprising:
reacting a compound of formula (X)
![]() wherein ring A is a di- or tri-substituted pyrazole, substituted on one ring nitrogen by RB2 and substituted on at least one ring carbon by RB3;
RB2 is C1-C3 alkyl or C1-C3fluoroalkyl;
n is an integer of 1 or 2,
each RB3 is independently halogen, C1-C3haloalkoxy, C1-C3haloalkyl, C1-C3alkoxy, or C1-C3alkyl;
RQ1 and RQ4 are each hydrogen; and
RQ2 and RQ3 together with the carbon atoms to which they are joined form ring Q, which is an optionally substituted 5-membered thio-lactam ring;
to produce a pharmaceutical or agrochemical having a pyrazolo-pyrrolidone motif.
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