HRID34158

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID6422

未命名化合物

结构：CN(C)C(On1nnc2ccccc21)=[N+](C)C.F[B-](F)(F)F

HCID2733207

O-(Benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate

C11H16BF4N5O

HCID5256896

2-(4-methyl-piperazin-1-ylmethyl)-piperidine

C11H23N3

结构：CC(C)(C)OC(=O)n1c(C(CCC(=O)O)Nc2ncnc3cc(C(=O)N4CCCC4)c(Cl)cc23)nc2cc(Cl)ccc21

HCID68938489

未命名化合物

PRODUCTS

生成物

结构：CN1CCN(CC2CCCCN2C(=O)CCC(Nc2ncnc3cc(C(=O)N4CCCC4)c(Cl)cc23)c2nc3cc(Cl)ccc3[nH]2)CC1

HCID178480824

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID22177404

未命名化合物

PROCEDURE

实验过程

Prepared analogously to Example 61 from 6-chloro-4-[1-(1-tert.-butyloxycarbonyl-5-chloro-1H-benzimidazol-2-yl)-3-hydroxycarbonyl-propyl-amino]-7-(pyrrolidin-1-yl-carbonyl)-quinazoline and 2-(4-methyl-piperazin-1-ylmethyl)-piperidine with TBTU in acetonitrile/tetrahydrofuran and subsequent reaction with trifluoroacetic acid.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-8c83c0e2f4634d18be8f9644272c32d6
来源数据集: uspto-grants-2008_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07429597B2
来源说明: uspto-grants-2008_09

反应 SMILES

[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[C:12]([N:14]1[CH2:18][CH2:17][CH2:16][CH2:15]1)=[O:13])[N:8]=[CH:7][N:6]=[C:5]2[NH:19][CH:20]([C:26]1[N:30](C(OC(C)(C)C)=O)[C:29]2[CH:38]=[CH:39][C:40]([Cl:42])=[CH:41][C:28]=2[N:27]=1)[CH2:21][CH2:22][C:23](O)=[O:24].[CH3:43][N:44]1[CH2:49][CH2:48][N:47]([CH2:50][CH:51]2[CH2:56][CH2:55][CH2:54][CH2:53][NH:52]2)[CH2:46][CH2:45]1.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.FC(F)(F)C(O)=O>C(#N)C.O1CCCC1>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[C:12]([N:14]1[CH2:18][CH2:17][CH2:16][CH2:15]1)=[O:13])[N:8]=[CH:7][N:6]=[C:5]2[NH:19][CH:20]([C:26]1[NH:30][C:29]2[CH:38]=[CH:39][C:40]([Cl:42])=[CH:41][C:28]=2[N:27]=1)[CH2:21][CH2:22][C:23]([N:52]1[CH2:53][CH2:54][CH2:55][CH2:56][CH:51]1[CH2:50][N:47]1[CH2:46][CH2:45][N:44]([CH3:43])[CH2:49][CH2:48]1)=[O:24]