HRID1919453

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID33557

未命名化合物

结构：CC(C)OC(=O)OC(OC(=O)[C@H](O[Si](C)(C)C(C)(C)C)C(C)(C)COS(=O)(=O)CCCCl)C(C)C

HCID86628921

未命名化合物

PRODUCTS

生成物

结构：CC(C)OC(=O)OC(OC(=O)[C@H](O[Si](C)(C)C(C)(C)C)C(C)(C)COS(=O)(=O)CCCN=[N+]=[N-])C(C)C

HCID86628922

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID679

Dimethyl sulfoxide

C2H6OS

PROCEDURE

实验过程

Following the general procedure for the preparation of azides of Description 16, a mixture of 2-methyl-1-(methylethoxycarbonyloxy)propyl (2R)-4-[(3-chloropropyl)sulfonyloxy]-3,3-dimethyl-2-(1,1,2,2-tetramethyl-1-silapropoxy)butanoate (47a) (0.6 g max.) dissolved in 5 mL of anhydrous dimethyl sulfoxide (DMSO) was reacted with 69 mg (1.1 mmol) of sodium azide (NaN3). After work-up, the crude title compound (47b) was used in the next step without further purification. MS (ESI) m/z 590.22 (M+Na)+.

WORKUP

后处理

customAfter work-up, the crude title compound (47b) was used in the next step without further purification

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-e93e36355303453ba427e2ff040a5b72
来源数据集: uspto-grants-2012_05
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08168617B2
来源说明: uspto-grants-2012_05

反应 SMILES

Cl[CH2:2][CH2:3][CH2:4][S:5]([O:8][CH2:9][C:10]([CH3:35])([CH3:34])[C@@H:11]([O:26][Si:27]([CH3:33])([CH3:32])[C:28]([CH3:31])([CH3:30])[CH3:29])[C:12]([O:14][CH:15]([O:19][C:20]([O:22][CH:23]([CH3:25])[CH3:24])=[O:21])[CH:16]([CH3:18])[CH3:17])=[O:13])(=[O:7])=[O:6].[N-:36]=[N+:37]=[N-:38].[Na+]>CS(C)=O>[N:36]([CH2:2][CH2:3][CH2:4][S:5]([O:8][CH2:9][C:10]([CH3:35])([CH3:34])[C@@H:11]([O:26][Si:27]([CH3:33])([CH3:32])[C:28]([CH3:31])([CH3:30])[CH3:29])[C:12]([O:14][CH:15]([O:19][C:20]([O:22][CH:23]([CH3:25])[CH3:24])=[O:21])[CH:16]([CH3:18])[CH3:17])=[O:13])(=[O:7])=[O:6])=[N+:37]=[N-:38]