HRID735651

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID15620607

Oxoacetic acid--water (1/1)

C2H4O4

结构：Cc1cc(B(O)O)ccc1CCOC(=O)Nc1cccc([C@H](C)NC(=O)OCc2ccccc2)c1

HCID57842831

未命名化合物

结构：CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)c1nccc2cc(N)ccc12

HCID58717298

未命名化合物

PRODUCTS

生成物

结构：Cc1cc(C(Nc2ccc3c(N(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)nccc3c2)C(=O)O)ccc1CCOC(=O)Nc1cccc([C@H](C)NC(=O)OCc2ccccc2)c1

HCID57842915

未命名化合物

收率 63%

PROCEDURE

实验过程

Using a procedure analogous to that used to prepare 2D, 59D (280 mg, 0.588 mmol) was reacted with Intermediate 1 and glyoxylic acid monohydrate to afford 59E (313 mg, 63%) as an oil. MS (ESI) m/z 848.7 (M+H)+.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-c46d8008e9084d8ebd3b8c41727f4a9e
来源数据集: uspto-grants-2009_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07592331B2
来源说明: uspto-grants-2009_09

反应 SMILES

[CH2:1]([O:8][C:9]([NH:11][C@H:12]([C:14]1[CH:15]=[C:16]([NH:20][C:21]([O:23][CH2:24][CH2:25][C:26]2[CH:31]=[CH:30][C:29](B(O)O)=[CH:28][C:27]=2[CH3:35])=[O:22])[CH:17]=[CH:18][CH:19]=1)[CH3:13])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:36][C:37]1[CH:38]=[C:39]2[C:44](=[CH:45][CH:46]=1)[C:43]([N:47]([C:55]([O:57][C:58]([CH3:61])([CH3:60])[CH3:59])=[O:56])[C:48]([O:50][C:51]([CH3:54])([CH3:53])[CH3:52])=[O:49])=[N:42][CH:41]=[CH:40]2.O.[C:63]([OH:67])(=[O:66])[CH:64]=O>>[CH2:1]([O:8][C:9]([NH:11][C@H:12]([C:14]1[CH:15]=[C:16]([NH:20][C:21]([O:23][CH2:24][CH2:25][C:26]2[CH:31]=[CH:30][C:29]([CH:64]([NH:36][C:37]3[CH:38]=[C:39]4[C:44](=[CH:45][CH:46]=3)[C:43]([N:47]([C:48]([O:50][C:51]([CH3:52])([CH3:53])[CH3:54])=[O:49])[C:55]([O:57][C:58]([CH3:61])([CH3:60])[CH3:59])=[O:56])=[N:42][CH:41]=[CH:40]4)[C:63]([OH:67])=[O:66])=[CH:28][C:27]=2[CH3:35])=[O:22])[CH:17]=[CH:18][CH:19]=1)[CH3:13])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1