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HRID368870

反应详情

EQUATION

反应方程式

HRID 368870 的结构方程式

REACTANTS

反应物

5
结构：NS(=O)(=O)c1ccc(N2CCNCC2)cc1
HCID901897

4-piperazin-1-ylbenzenesulfonamide

C10H15N3O2S

结构：O=C(O)CC1OCCc2ccccc21
HCID13308864

(3,4-Dihydro-1H-2-benzopyran-1-yl)acetic acid

C11H12O3

结构：CC1CN(c2ccc(C(N)=O)cc2)CC(C)N1
HCID23288921

未命名化合物

结构：CC1COC(CCCl)c2ccccc21
HCID23288938

未命名化合物

结构：CC(C(=O)N1C(=O)OC[C@@H]1Cc1ccccc1)c1ccccc1
HCID56980759

(4S)-4-(phenylmethyl)-3-(2-phenylpropionyl)-2-oxazolidinone

C19H19NO3

PRODUCTS

生成物

1
结构：C[C@@H]1CN(c2ccc(C(N)=O)cc2)C[C@H](C)N1CC[C@@H]1OCCc2ccccc21
HCID15487843

(S)-(-)-4-[4-[2-(Isochroman-1-yl)ethyl]-cis-3,5-dimethylpiperazin-1-yl]benzamide

C24H31N3O2

PROCEDURE

实验过程

Following the general procedure of EXAMPLE 48 and making non-critical variations (-)-isochromanylacetic acid (LXI, EXAMPLE 45, 0.346 g) and 4-(3,5-dimethylpiperazin-1-yl)benzamide [(IV), 0.462 g; prepared from 4-fluorobenzamide (III) and cis-2,6-dimethylpiperazine (II, Aldrich) by the procedure of EXAMPLE 47, Step 1] gives the title compound, mp 206-207°; MS (m/z) 393; IR (mineral oil) 1640, 1607, 1246, 3383, 1402, 1395, 1422, 1112 and 1332 cm-1.