HRID1493406

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID77202

2,4,8,10-Tetraoxa-3,9-diphosphaspiro[5.5]undecane, 3,9-dichloro-

C5H8Cl2O4P2

结构：CCCCNC1CC(C)(C)N(OC(C)c2ccccc2)C(C)(C)C1

HCID19768373

未命名化合物

PRODUCTS

生成物

结构：CCCCN(C1CC(C)(C)N(OC(C)c2ccccc2)C(C)(C)C1)P1OCC2(CO1)COP(N(CCCC)C1CC(C)(C)N(OC(C)c3ccccc3)C(C)(C)C1)OC2

HCID57182020

未命名化合物

PROCEDURE

实验过程

The title compound is prepared as a viscous syrup from 4-n-butylamino-1-alpha-methylbenzyloxy-2,2,6,6-tetramethylpiperidine (made in Example 13A) and 3,9-dichloro-2,4,8,10-tetraoxa-3, 9-diphosphaspiro[5.5]undecane according to the procedure of Example 14.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-cf9282fb269c4b52a0a1c5e83c420caf
来源数据集: uspto-grants-1991_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05021481
来源说明: uspto-grants-1991_06

反应 SMILES

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