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X-ray crystallographic analysis of C21H32N 2O3S was performed at 223(2) K by using a STOE IPDS II diffractometer with MoKα radiation (λ, 0.71073 Å) and a graphite monochromator. Crystal system: triclinic, P 1 (No. 2, Z, 1, a, 632.32(13) pm, b, 900.7(2) pm, c, 1935.2(4) pm, α, 84.236(19, β, 83.827(17, γ, 77.126(18, VEZ, 1064.9(4) 106 pm3. The structure was solved by direct methods (SHELXS-97)10a using 3704 independent reflections. Structure refinement: full matrix least-squares methods on F2 using SHELXL-9710b all nonhydrogen atoms with anisotropic displacement parameters. All hydrogen atoms were taken from a difference Fourier synthesis and were isotropically refined. The refinement converged to a final wR2, 0.1223 for 3704 unique reflections and R1, 0.0540 for 2420 observed reflections
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