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HRID1279046

反应详情

EQUATION

反应方程式

HRID 1279046 的结构方程式

REACTANTS

反应物

2
结构：CCCCCCCCS(=O)(=O)Cl
HCID82261

1-Octanesulfonyl chloride

C8H17ClO2S

结构：CC1CCN(C(=O)C(Cc2cc3c(N)nccc3s2)NS(=O)(=O)c2ccc(OC3CCOCC3)cc2)CC1
HCID22665795

N-[1-(4-Amino-thieno[3,2-c]pyridin-2-ylmethyl)-2-(4-methyl-piperidin-1-yl)-2-oxo-ethyl]-4-(tetrahydropyran-4-yloxy)-benzenesulfonamide

C27H34N4O5S2

PRODUCTS

生成物

1
结构：CCCCCCCCS(=O)(=O)NC(Cc1cc2c(N)nccc2s1)C(=O)N1CCC(C)CC1
HCID86758421

未命名化合物

PROCEDURE

实验过程

This compound was prepared from 0.15 mL of octane sulfonyl chloride and 210 mg of 30a using the procedure described for 58c. Yield: 150 mg; m.p. 101-112° C., (+)-FAB-MS: 495 (MH+).