HRID71765

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：COC(=O)NC(C(=O)N1CCCC1c1ncc(-c2ccc(-c3ccc(-c4cnc(CN5CCCC(NC(=O)OC(C)(C)C)C5=O)[nH]4)cc3)cc2)[nH]1)C(C)C

HCID66620320

未命名化合物

结构：COC(=O)NC(C(=O)N1CCCC1c1nc(-c2ccc(C#Cc3ccc(-c4cn(COCC[Si](C)(C)C)c(C5CN(C(=O)OC(C)(C)C)CN5C(=O)C(NC(=O)OC)C(C)C)n4)cc3)cc2)cn1COCC[Si](C)(C)C)C(C)C

HCID86648880

未命名化合物

PRODUCTS

生成物

结构：COC(=O)NC(C(=O)N1CCCC1c1nc(-c2ccc(C#Cc3ccc(-c4cn(COCC[Si](C)(C)C)c(C5CNCN5C(=O)C(NC(=O)OC)C(C)C)n4)cc3)cc2)cn1COCC[Si](C)(C)C)C(C)C

HCID86648881

未命名化合物

PROCEDURE

实验过程

3′-(2-Methoxycarbonylamino-3-methyl-butyryl)-4-[4-(4-{2-[1-(2-methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-4-yl}-phenylethynyl)-phenyl]-1-(2-trimethylsilanyl-ethoxymethyl)-2′,3′,4′,5′-tetrahydro-1H-[2,4′]biimidazole was prepared using method 804 substituting 3′-(2-methoxycarbonylamino-3-methyl-butyryl)-4-[4-(4-{2-[1-(2-methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazol-4-yl}-phenylethynyl)-phenyl]-1-(2-trimethylsilanyl-ethoxymethyl)-2′,3′,4′,5′-tetrahydro-1H-[2,4′]biimidazolyl-1′-carboxylic acid tert-butyl ester for {1-[5-(4′-{2-[1-(2-Methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-3H-imidazol-4-yl}-biphenyl-4-yl)-1H-imidazol-2-ylmethyl]-2-oxo-piperidin-3-yl}-carbamic acid tert-butyl ester. C53H77N9O8Si2 calculated 1023.5 observed [M+1]+ 1024.7; rt=2.81 min.

WORKUP

后处理

customrt=2.81 min.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-5e0f41c1eecc430dbd5a5ab7f5da0320
来源数据集: uspto-grants-2014_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08822430B2
来源说明: uspto-grants-2014_09

反应 SMILES

C(OC([N:8]1[CH2:12][CH:11]([C:13]2[N:14]([CH2:61][O:62][CH2:63][CH2:64][Si:65]([CH3:68])([CH3:67])[CH3:66])[CH:15]=[C:16]([C:18]3[CH:23]=[CH:22][C:21]([C:24]#[C:25][C:26]4[CH:31]=[CH:30][C:29]([C:32]5[N:33]=[C:34]([CH:45]6[CH2:49][CH2:48][CH2:47][N:46]6[C:50](=[O:60])[CH:51]([NH:55][C:56]([O:58][CH3:59])=[O:57])[CH:52]([CH3:54])[CH3:53])[N:35]([CH2:37][O:38][CH2:39][CH2:40][Si:41]([CH3:44])([CH3:43])[CH3:42])[CH:36]=5)=[CH:28][CH:27]=4)=[CH:20][CH:19]=3)[N:17]=2)[N:10]([C:69](=[O:79])[CH:70]([NH:74][C:75]([O:77][CH3:78])=[O:76])[CH:71]([CH3:73])[CH3:72])[CH2:9]1)=O)(C)(C)C.C(OC(=O)NC1CCCN(CC2NC(C3C=CC(C4C=CC(C5NC(C6CCCN6C(=O)C(NC(OC)=O)C(C)C)=NC=5)=CC=4)=CC=3)=CN=2)C1=O)(C)(C)C>>[CH3:78][O:77][C:75]([NH:74][CH:70]([CH:71]([CH3:73])[CH3:72])[C:69]([N:10]1[CH:11]([C:13]2[N:14]([CH2:61][O:62][CH2:63][CH2:64][Si:65]([CH3:68])([CH3:67])[CH3:66])[CH:15]=[C:16]([C:18]3[CH:23]=[CH:22][C:21]([C:24]#[C:25][C:26]4[CH:27]=[CH:28][C:29]([C:32]5[N:33]=[C:34]([CH:45]6[CH2:49][CH2:48][CH2:47][N:46]6[C:50](=[O:60])[CH:51]([NH:55][C:56]([O:58][CH3:59])=[O:57])[CH:52]([CH3:54])[CH3:53])[N:35]([CH2:37][O:38][CH2:39][CH2:40][Si:41]([CH3:42])([CH3:43])[CH3:44])[CH:36]=5)=[CH:30][CH:31]=4)=[CH:20][CH:19]=3)[N:17]=2)[CH2:12][NH:8][CH2:9]1)=[O:79])=[O:76]