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Diversification of Sulfinamide Moiety and Library Cleavage. With these 10 classes of scaffolds in hand, we next investigated diversification of the tert-butylsulfinamide moieties. We had originally selected this lynchpin in part because of its known acid-lability (40), and were pleased to find that the support-bound sulfinamides could be cleaved with HCl [1 M in dioxane/THF, room temperature (RT)] to afford the corresponding secondary amines without compromising the TBDAS linker (Scheme 2). This result opens the door for additional diversification of this position in the future (N-acylation, N-alkylation, etc.). Alternatively, treatment of the sulfinamides with meta-chloroperbenzoic acid (m-CPBA) (CH2Cl2, 0 ¡ãC) also provided the corresponding tert-butylsulfonamides efficiently.
Accordingly, seven scaffolds (5, 6, 8, 26¨C29) were produced with three variations at this position (amine, sulfinamide, sulfonamide). Three scaffolds required prior oxidation to the tertbutylsulfonamide to enable the cycloaddition reactions (7, 9, 10) and were limited to this functionality because it could not be cleaved effectively under a variety of conditions (e.g., PhSH, K2CO3; TFA, anisole; TfOH, anisole).

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