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HRID1815067

反应详情

EQUATION

反应方程式

HRID 1815067 的结构方程式

REACTANTS

反应物

3
结构：CCO
HCID702

Ethanol

C2H6O

结构：Cl.Cl.c1ccc(OC2CCNCC2)nc1
HCID14674154

Pyridine, 2-(4-piperidinyloxy)-, hydrochloride (1:2)

C10H16Cl2N2O

结构：CC(C)(C)OC(=O)N1CCC(Oc2ccncc2)CC1
HCID21906087

Tert-butyl 4-(pyridin-4-yloxy)piperidine-1-carboxylate

C15H22N2O3

PRODUCTS

生成物

1
结构：Cl.Cl.c1cc(OC2CCNCC2)ccn1
HCID17749787

4-[(Piperidin-4-yl)oxy]pyridine--hydrogen chloride (1/2)

C10H16Cl2N2O

AUXILIARIES

试剂、催化剂与溶剂

1
结构：CCOCC
溶剂HCID3283

Diethyl Ether

C4H10O

PROCEDURE

实验过程

Prepared from 1-Boc-4-(pyridin-4-yloxy)piperidine using methods substantially equivalent to those described for the synthesis of 4-(pyridin-2-yloxy)piperidine dihydrochloride, using ethanol in place of ethyl acetate. The product was isolated by trituration with diethyl ether.