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【结 构 式】

【分子编号】37001

【品名】1-(2-chloroethyl)-3-phenyl-2-imidazolidinone

【CA登记号】

【 分 子 式 】C11H13ClN2O

【 分 子 量 】224.6898

【元素组成】C 58.8% H 5.83% Cl 15.78% N 12.47% O 7.12%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(V)

Condensation of phenyl isocyanate (I) with diethanolamine (II) produced 1,1-bis(2-hydroxyethyl)-3-phenylurea (III), which was converted into the bis(chloroethyl) derivative (IV) upon treatment with SOCl2. Cyclization of this compound at 140 C furnished imidazolinone (V). Finally, condensation of (V) with benzisoxazolylpiperidine (VI) in the presence of K2CO3 and KI in refluxing methyl isobuyl ketone yielded the title compound.

1 Audinot, V.; Millan, M.; Brocco, M.; Peglion, J.-L. (ADIR et Cie.); 3-(Piperid-4-yl)-1,2-benzisoxazole and 3-(piperazin-4-yl)-1,2-benzisoxazole cpds.. EP 0811622; FR 2749304; US 5780474 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 11289 1-Isocyanatobenzene; phenyl isocyanate; Phenylisocyanate 103-71-9 C7H5NO 详情 详情
(II) 24273 2-[(2-hydroxyethyl)amino]-1-ethanol 111-42-2 C4H11NO2 详情 详情
(III) 36999 N,N-bis(2-hydroxyethyl)-N'-phenylurea C11H16N2O3 详情 详情
(IV) 37000 N,N-bis(2-chloroethyl)-N'-phenylurea C11H14Cl2N2O 详情 详情
(V) 37001 1-(2-chloroethyl)-3-phenyl-2-imidazolidinone C11H13ClN2O 详情 详情
(VI) 17910 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole C12H13FN2O 详情 详情
Extended Information