HRID1712633

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID46835223

6-(Chloromethyl)-4-(3-methoxypropyl)-2H-1,4-benzoxazin-3(4H)-one

C13H16ClNO3

结构：O=C(OCc1ccccc1)N1CCC(c2ccc(Oc3ccccc3)cc2)C(O)C1

HCID68500131

未命名化合物

PRODUCTS

生成物

结构：COCCCN1C(=O)COc2ccc(COC3CN(C(=O)OCc4ccccc4)CCC3c3ccc(Oc4ccccc4)cc3)cc21

HCID68503214

未命名化合物

PROCEDURE

实验过程

Analogously to Method D, 0.100 g of benzyl 3-hydroxy-4-(4-phenoxyphenyl)piperidine-1-carboxylate and 0.0753 g of 6-chloromethyl-4-(3-methoxypropyl)-4H-benzo[1,4]oxazin-3-one are reacted. The title compound is obtained as a colourless resin. Rf=0.31 (1:1 EtOAc-heptane); Rt=5.74.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-a469653dcfd7452db69024ea5566a7d9
来源数据集: uspto-grants-2010_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07790715B2
来源说明: uspto-grants-2010_09

反应 SMILES

[OH:1][CH:2]1[CH:7]([C:8]2[CH:13]=[CH:12][C:11]([O:14][C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)=[CH:10][CH:9]=2)[CH2:6][CH2:5][N:4]([C:21]([O:23][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[O:22])[CH2:3]1.Cl[CH2:32][C:33]1[CH:34]=[CH:35][C:36]2[O:41][CH2:40][C:39](=[O:42])[N:38]([CH2:43][CH2:44][CH2:45][O:46][CH3:47])[C:37]=2[CH:48]=1>>[CH3:47][O:46][CH2:45][CH2:44][CH2:43][N:38]1[C:37]2[CH:48]=[C:33]([CH2:32][O:1][CH:2]3[CH:7]([C:8]4[CH:9]=[CH:10][C:11]([O:14][C:15]5[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=5)=[CH:12][CH:13]=4)[CH2:6][CH2:5][N:4]([C:21]([O:23][CH2:24][C:25]4[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=4)=[O:22])[CH2:3]3)[CH:34]=[CH:35][C:36]=2[O:41][CH2:40][C:39]1=[O:42]