HRID36557

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID72655

1H,5H,11H-[1]Benzopyrano[6,7,8-ij]quinolizin-11-one, 10-acetyl-2,3,6,7-tetrahydro-

C17H17NO3

HCID688763

2H-1-Benzopyran-2-one, 3-acetyl-7-(diethylamino)-

C15H17NO3

PRODUCTS

生成物

结构：CCN(CCN1CCCCC1)c1ccc(C=CC(=O)c2cc3cc4c5c(c3oc2=O)CCCN5CCC4)cc1

HCID54085069

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID702

Ethanol

C2H6O

PROCEDURE

实验过程

10-(3-(N-ethyl-N-(2-piperidinoethyl)-4-aminophenyl)propenoyl)-1H,2H,3H,5H,6H,7H,11H-[1]benzopyrano[6,7,8-ij]quinolizin-11-one (7) was prepared according to the procedure of Example 3 wherein 3-acetyl-7-diethylaminocoumarin was replaced by Coumarin 334; (Eastman Kodak, Rochester, N.Y.) λmax (ethanol)=503 nm ##STR14##

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-65a8d59987b24ee7af10a32aaae06db0
来源数据集: uspto-grants-1995_05
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05415976
来源说明: uspto-grants-1995_05

反应 SMILES

C(C1C(=O)O[C:7]2[C:12]([CH:13]=1)=[CH:11][CH:10]=[C:9]([N:14]([CH2:17][CH3:18])[CH2:15][CH3:16])[CH:8]=2)(=O)C.[CH3:20][C:21]([C:23]1[C:32](=[O:33])[O:31][C:30]2[C:25](=[CH:26][C:27]3[CH2:40][CH2:39][CH2:38][N:37]4[C:28]=3[C:29]=2[CH2:34][CH2:35][CH2:36]4)[CH:24]=1)=[O:22]>C(O)C>[CH2:17]([N:14]([CH2:15][CH2:16][N:37]1[CH2:28][CH2:29][CH2:34][CH2:35][CH2:36]1)[C:9]1[CH:8]=[CH:7][C:12]([CH:13]=[CH:20][C:21]([C:23]2[C:32](=[O:33])[O:31][C:30]3[C:25](=[CH:26][C:27]4[CH2:40][CH2:39][CH2:38][N:37]5[C:28]=4[C:29]=3[CH2:34][CH2:35][CH2:36]5)[CH:24]=2)=[O:22])=[CH:11][CH:10]=1)[CH3:18]