反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A solution of (15R,19R)-tert-butyl 15-amino-19-(decylcarbamoyloxy)-14,22-dioxo-4,7,10,21-tetraoxa-17-thia-13,23-diazatritriacontan-1-oate in 30% TFA in DCM (0.3 M) was stirred at room temperature until complete deprotection of the tert-butyl group (4 hours). The reaction was diluted with DCM and concentrated with a stream of nitrogen then purified by flash chromatography on a COMBIFLASH® system (ISCO) using a gradient of 0-10% MeOH/DCM with 0.5% AcOH to afford (15R,19R)-15-amino-19-(decylcarbamoyloxy)-14,22-dioxo-4,7,10,21-tetraoxa-17-thia-13,23-diazatritriacontan-1-oic acid as a clear oil. 1H NMR (DMSO-d6): δ 12.21 (br s, 1H), 8.22 (t, 1H), 7.23 (m, 2H), 4.92 (m, 1H), 4.18 (dd, 2H), 3.94 (m, 1H), 3.57 (t, 2H), 3.30-3.54 (m, 12H), 3.37 (t, 2H), 2.90-3.08 (m, 4H), 2.60-2.82 (m, 4H), 2.48 (t, 2H), 1.32 (m, 4H), 1.22-1.28 (m, 28H), 0.79 (t, 6H). LRMS [M+H]=765.5.
WORKUP
后处理
- concentrationconcentrated with a stream of nitrogen
- customthen purified by flash chromatography on a COMBIFLASH® system (ISCO)