It is important to note the difference between instantaneous spontineaity and overall reaction spontineaity. The values you cited for del(H)rxn and del(S)rxn correspond to overall reaction changes (i.e. converting one molar equivalent of pure reactants at standard conditions to one molar equivalent of products at standard conditions) the enthalpy and entropy changes for this process is a constant for the reaction, since they refer the the specific process noted in the parenthases which dictates the reaction conditions exactly.
However, instantaneous values need to be adjusted for concentrations (via Q) and temperature via del(G)=del(G)rxn + RTln(Q). The del(G) (without the rxn subtitle) pertains to instantaneous spontinaeity (i.e. spontineaty at any instant, given values for Q and T) whereas the del(G)rxn refers to the overall reaction spontineaity (the process I described in the first parentheses, i.e. a constant for the reaction).
So as Lechatlier stated, you must apply the stress to a system already at equilibrium. If the system you described has a negative value of del(G)rxn as noted correctly by the previous posters, then at equilibrium ( please note at equilibrium del(g)=0) this dictates RTln(Q) must be positive. If the system is closed (i.e. no mass enters or exits), Q will not vary, but as T goes up del(G) must go up. Therefore the reaction becomes instantaneously nonspontaneous.
Now on to exothermic. del(H) (the instantaneous enthalpy change) essentially only depends on the systems change in potential energy (H=U+PV) for a constant pressure/volume system the potential energy change will determine the instantaneous enthalpy change. Since the potential energy of reactants going to products is the same no matter what the composition of reactant or products is, the enthalpy change will remain negative (and therefore exothermic) no matter whether the system is at equilibrium/reactant heavey/ or product heavey.
