The invention relates to a compound of formula (1); wherein: R.sup.1 and
R.sup.2 each independently represent a C.sub.1-6alkyl, C.sub.3-6 alkenyl,
C.sub.3-6 cycloalkyl C.sub.1-3 alkyl or C.sub.3-6 cycloalkyl; each of
which may be optionally substituted by 1 to 3 halogen atoms; R.sup.3 is
isoxyzolidin-2-ylcarbonyl or tetrahydroisoxazin-2-ylcarbonyl wherein each
ring is optionally substituted by one hydroxy group; Q is CO-- or
C(R.sup.4)(R.sup.5)-(wherein R.sup.4 is a hydrogen atom or C.sub.1-4alkyl
and R.sup.5 is a hydrogen atom or hydroxy group); Ar is a 5- to
10-membered aromatic ring system wherein up to 4 ring atoms may be
heteroatoms independently selected from nitrogen, oxygen and sulphur, the
ring system being optionally substituted by one or more substituents as
defined in the specification. It also relates to methods of preparing,
pharmaceutical compositions containing and methods of using the compound
of the formula (1), particularly in the modulation of autoimmune disease
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