HRID2253674

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID11776

Triphenylphosphine

C18H15P

HCID220568

ethyl N-ethoxycarbonyliminocarbamate

C6H10N2O4

HCID15105369

未命名化合物

结构：O=C(c1ccc(F)cc1)C1(c2ccccc2)CCN(CCO)CC1

HCID19746014

未命名化合物

PRODUCTS

生成物

结构：O=C(c1ccc(F)cc1)C1(c2ccccc2)CCN(CCn2c(=O)nc3n(c2=O)CCCC3)CC1

HCID19745975

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID6228

N,N-Dimethylformamide

C3H7NO

PROCEDURE

实验过程

In the manner described in Example 1-2), 6,7,8,9-tetrahydro-2H-pyrido[1,2-a]-1,3,5-triazine-2,4(3H)-dione obtained in Example 1-1) and 4-(4-fluorobenzoyl)-4-phenyl-1-(2-hydroxyethyl)piperidine were condensed in N,N-dimethylformamide in the presence of triphenylphosphine and diethyl azodicarboxylate to obtain the entitled compound as an oily substance.

WORKUP

后处理

customto obtain the entitled compound as an oily substance

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-55df493a0210447490038d44777d0315
来源数据集: uspto-grants-1993_08
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05232924
来源说明: uspto-grants-1993_08

反应 SMILES

[N:1]1[C:6](=[O:7])[NH:5][C:4](=[O:8])[N:3]2[CH2:9][CH2:10][CH2:11][CH2:12][C:2]=12.[F:13][C:14]1[CH:36]=[CH:35][C:17]([C:18]([C:20]2([C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=3)[CH2:25][CH2:24][N:23]([CH2:26][CH2:27]O)[CH2:22][CH2:21]2)=[O:19])=[CH:16][CH:15]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OCC)=O)=NC(OCC)=O>CN(C)C=O>[F:13][C:14]1[CH:15]=[CH:16][C:17]([C:18]([C:20]2([C:29]3[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=3)[CH2:25][CH2:24][N:23]([CH2:26][CH2:27][N:5]3[C:4](=[O:8])[N:3]4[CH2:9][CH2:10][CH2:11][CH2:12][C:2]4=[N:1][C:6]3=[O:7])[CH2:22][CH2:21]2)=[O:19])=[CH:35][CH:36]=1