HRID460636

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8857

Ethyl acetate

C4H8O2

HCID15435

Ethanone, 1-(2-benzofuranyl)-

C10H8O2

$结构：O=C(O)/C=C\C(=O)O$

HCID444266

Maleic acid

C4H4O4

HCID22029264

4-(Naphthalen-2-yl)piperidine

C15H17N

PRODUCTS

生成物

$结构：CC(=O)c1cc2c(OC[C@@H](O)CN3CCC(c4ccc5ccccc5c4)CC3)cccc2o1.O=C(O)/C=C\C(=O)O$

HCID69497711

未命名化合物

PROCEDURE

实验过程

By the reactions in the same manner as in Example 3 using (S)-4-glycidyloxybenzo(b)furan-2-yl methyl ketone (0.52 g) obtained in Starting Material Synthesis Example 71 and 4-(naphthalen-2-yl)piperidine (0.47 g), (S)-4-(2-hydroxy-3-(4-naphthalen-2-yl)piperidino)propyloxy)benzo(b)furan-2-yl methyl ketone (0.87 g) was obtained as a brown oil. This was dissolved in ethyl acetate and maleic acid (0.22 g) was added. The precipitated crystals were recrystallized from a mixed solvent of isopropanol-ethyl acetate to give the title compound (0.76 g) as pale-yellow crystals, melting point 153–155° C.

WORKUP

后处理

customwas obtained as a brown oil
customThe precipitated crystals were recrystallized from a mixed solvent of isopropanol-ethyl acetate

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-0fc6302ec1ee4ea392d094007397ede9
来源数据集: uspto-grants-2007_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07196199B2
来源说明: uspto-grants-2007_03

反应 SMILES

[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH:11]1[CH2:16][CH2:15][NH:14][CH2:13][CH2:12]1.[CH3:17][C:18]([C:20]1[O:24][C:23]2[CH:25]=[CH:26][CH:27]=[CH:28][C:22]=2[CH:21]=1)=[O:19].[C:29]([OH:36])(=[O:35])/[CH:30]=[CH:31]\[C:32]([OH:34])=[O:33].C([O:40][CH2:41][CH3:42])(=O)C>>[C:29]([OH:36])(=[O:35])/[CH:30]=[CH:31]\[C:32]([OH:34])=[O:33].[CH3:17][C:18]([C:20]1[O:24][C:23]2[CH:25]=[CH:26][CH:27]=[C:28]([O:33][CH2:32][C@@H:41]([OH:40])[CH2:42][N:14]3[CH2:15][CH2:16][CH:11]([C:2]4[CH:3]=[CH:4][C:5]5[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=5)[CH:1]=4)[CH2:12][CH2:13]3)[C:22]=2[CH:21]=1)=[O:19]