HRID1642571
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
The title compound was synthesized from Compound 157 and 2-(benzyloxy)ethanol using an analogous procedure to that outlined in the preparation of Compound 210 followed by debenzylation using Pd/C—H2. 1H NMR (400 MHz, Methanol-d4) δ 8.30 (s, 1 H) 8.19 (m, 1 H) 8.06 (m, 1 H) 8.00 (m, 2 H) 7.87 (t, J=8.0 Hz, 1 H) 7.26 (m, 2 H) 4.38 (t, J=4 Hz, 2 H) 4.08 (t, J=4 Hz, 2 H) 3.30 (q, J=7.5 Hz, 2 H) 2.41 (s, 3 H) 1.31 (t, J=7.5 Hz, 3 H). [M+H] calc'd for C22H23N2O4S, 411; found, 411.