HRID1281501

反应详情

EQUATION

反应方程式

REACTANTS

反应物

反应SMILES：CC(C)(C)[Si](Oc1ccc(OCC2CO2)cc1)(c1ccccc1)c1ccccc1

HCID12045564

未命名化合物

反应SMILES：COc1ccc(C2CCN(C(=O)N3CCC(Nc4ccc(CCN)cc4)CC3)CC2)cc1OC1CCCC1.O=CO

HCID69985596

未命名化合物

PRODUCTS

产物

反应SMILES：COc1ccc(C2CCN(C(=O)N3CCC(Nc4ccc(CCNC[C@H](O)COc5ccc(O)cc5)cc4)CC3)CC2)cc1OC1CCCC1

HCID10233652

未命名化合物

收率 20.6%

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID21584188

Chloroform methanol

C2H5Cl3O

PROCEDURE

实验过程

{4-[4-(2-Aminoethyl)anilino]-1-piperidinyl}{4-[3-(cyclopentyloxy)-4-methoxyphenyl]-1-piperidinyl}methanone formate (0.50 g, 0.88 mmol) was reacted with tert-butyl-(4-oxiranylmethoxy-phenoxy)-diphenyl-silane (0.350 g, 0.88 mmol) according to Procedure G to yield (eluant: 20:1 chloroform-methanol) the title compound (0.168 g, 0.181 mmol)

来源与证据

来源类型: Open Reaction Database
ORD记录: ord-ace2c4fbbb1c4326a269bffc1a0cf883
来源数据集: uspto-grants-2002_09
DOI: 10.6084/m9.figshare.5104873.v1
专利号: US06451814B1
来源说明: uspto-grants-2002_09

反应SMILES

C(O)=O.[NH2:4][CH2:5][CH2:6][C:7]1[CH:41]=[CH:40][C:10]([NH:11][CH:12]2[CH2:17][CH2:16][N:15]([C:18]([N:20]3[CH2:25][CH2:24][CH:23]([C:26]4[CH:31]=[CH:30][C:29]([O:32][CH3:33])=[C:28]([O:34][CH:35]5[CH2:39][CH2:38][CH2:37][CH2:36]5)[CH:27]=4)[CH2:22][CH2:21]3)=[O:19])[CH2:14][CH2:13]2)=[CH:9][CH:8]=1.C([Si]([O:59][C:60]1[CH:65]=[CH:64][C:63]([O:66][CH2:67][CH:68]2[CH2:70][O:69]2)=[CH:62][CH:61]=1)(C1C=CC=CC=1)C1C=CC=CC=1)(C)(C)C>C(Cl)(Cl)Cl.CO>[CH:35]1([O:34][C:28]2[CH:27]=[C:26]([CH:23]3[CH2:22][CH2:21][N:20]([C:18]([N:15]4[CH2:14][CH2:13][CH:12]([NH:11][C:10]5[CH:40]=[CH:41][C:7]([CH2:6][CH2:5][NH:4][CH2:70][C@H:68]([OH:69])[CH2:67][O:66][C:63]6[CH:64]=[CH:65][C:60]([OH:59])=[CH:61][CH:62]=6)=[CH:8][CH:9]=5)[CH2:17][CH2:16]4)=[O:19])[CH2:25][CH2:24]3)[CH:31]=[CH:30][C:29]=2[O:32][CH3:33])[CH2:36][CH2:37][CH2:38][CH2:39]1