HRID2406153

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID1110

Butanedioic acid

C4H6O4

$结构：CCCN(CCC)C(=O)COC(=O)CCNS(=O)(=O)c1cccc(C(=O)N2CCC3(CC2)CN/C(=N\C(=O)c2nc(Cl)c(N)nc2N)N3)c1$

HCID178457291

未命名化合物

PRODUCTS

生成物

$结构：CCCN(CCC)C(=O)COC(=O)CCNS(=O)(=O)c1cccc(C(=O)N2CCC3(CC2)CN/C(=N\C(=O)c2nc(Cl)c(N)nc2N)N3)c1.O=C(O)CCC(=O)O$

HCID178457292

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID6569

Methyl ethyl ketone

C4H8O

CONDITIONS

反应条件

温度: 20 °C

PROCEDURE

实验过程

0.535 g of 3-(3-{2-[(E)-3,5-Diamino-6-chloro-pyrazine-2-carbonylimino]-1,3,8-triaza-spiro[4.5]decane-8-carbonyl}-benzenesulfonylamino)-propionic acid dipropylcarbamoylmethyl ester (may be prepared as in Preparation 1) and 0.12 g succinic acid were dissolved in 7.27 g methyl ethyl ketone at 60° C. in a magnetically stirred glass vial. The solution was cooled to 20° C. and then stirred at this temperature overnight. The resulting suspension was filtered.

WORKUP

后处理

filtrationThe resulting suspension was filtered

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-9f65537836204f68903552a4bfd5b32a
来源数据集: uspto-grants-2014_08
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08809340B2
来源说明: uspto-grants-2014_08

反应 SMILES

[CH2:1]([N:4]([CH2:47][CH2:48][CH3:49])[C:5]([CH2:7][O:8][C:9](=[O:46])[CH2:10][CH2:11][NH:12][S:13]([C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([C:22]([N:24]2[CH2:45][CH2:44][C:27]3([NH:31]/[C:30](=[N:32]/[C:33]([C:35]4[C:40]([NH2:41])=[N:39][C:38]([NH2:42])=[C:37]([Cl:43])[N:36]=4)=[O:34])/[NH:29][CH2:28]3)[CH2:26][CH2:25]2)=[O:23])[CH:17]=1)(=[O:15])=[O:14])=[O:6])[CH2:2][CH3:3].[C:50]([OH:57])(=[O:56])[CH2:51][CH2:52][C:53]([OH:55])=[O:54]>C(C(C)=O)C>[C:50]([OH:57])(=[O:56])[CH2:51][CH2:52][C:53]([OH:55])=[O:54].[CH2:47]([N:4]([CH2:1][CH2:2][CH3:3])[C:5]([CH2:7][O:8][C:9](=[O:46])[CH2:10][CH2:11][NH:12][S:13]([C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([C:22]([N:24]2[CH2:45][CH2:44][C:27]3([NH:31]/[C:30](=[N:32]/[C:33]([C:35]4[C:40]([NH2:41])=[N:39][C:38]([NH2:42])=[C:37]([Cl:43])[N:36]=4)=[O:34])/[NH:29][CH2:28]3)[CH2:26][CH2:25]2)=[O:23])[CH:17]=1)(=[O:15])=[O:14])=[O:6])[CH2:48][CH3:49]