HRID1397560

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID11430

Potassium Carbonate

CK2O3

结构：CC1(C)O[C@@H]2[C@@H](CO[Si](C)(C)C(C)(C)C)C[C@@H](N)[C@@H]2O1

HCID66798191

未命名化合物

HCID86618715

未命名化合物

PRODUCTS

生成物

结构：Cc1nc(N[C@H]2CCc3ccccc32)nc(N[C@@H]2C[C@@H](CO[Si](C)(C)C(C)(C)C)[C@H]3OC(C)(C)O[C@H]32)n1

HCID66797981

未命名化合物

收率 24.3%

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID31275

1,4-Dioxane

C4H8O2

PROCEDURE

实验过程

A mixture of (3aS,4R,6R,6aR)-6-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-amine (141.8 mg, 0.0004703 mol), 4-chloro-N-[(1S)-2,3-dihydro-1H-inden-1-yl]-6-methyl-1,3,5-triazin-2-amine (127.1 mg, 0.0004876 mol) and potassium carbonate (0.130 g, 0.000940 mol) in 1,4-dioxane (0.77 mL) was subjected to microwave irradiation (300 watts, 160° C.) for 30 minutes. The mixture was filtered with CH2Cl2 and concentrated. The residue was purified by flash chromatography (10 to 100% EtOAc/hexanes) to obtain 60 mg (24%) of the title compound. LC/MS: Rt=2.03 min, ES+ 279 (FA standard).

WORKUP

后处理

customwas subjected to microwave irradiation (300 watts, 160° C.) for 30 minutes
filtrationThe mixture was filtered with CH2Cl2
concentrationconcentrated
customThe residue was purified by flash chromatography (10 to 100% EtOAc/hexanes)

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-b9b045c452fa47ec8c3a0ae7fda2937e
来源数据集: uspto-grants-2014_12
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08901136B2
来源说明: uspto-grants-2014_12

反应 SMILES

[Si:1]([O:8][CH2:9][C@@H:10]1[C@H:14]2[O:15][C:16]([CH3:19])([CH3:18])[O:17][C@H:13]2[C@H:12]([NH2:20])[CH2:11]1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].Cl[C:22]1[N:27]=[C:26]([CH3:28])[N:25]=[C:24]([NH:29][C@@H:30]2[C:38]3[C:33](=[CH:34][CH:35]=[CH:36][CH:37]=3)[CH2:32][CH2:31]2)[N:23]=1.C(=O)([O-])[O-].[K+].[K+]>O1CCOCC1>[Si:1]([O:8][CH2:9][C@H:10]1[C@H:14]2[O:15][C:16]([CH3:19])([CH3:18])[O:17][C@H:13]2[C@H:12]([NH:20][C:22]2[N:23]=[C:24]([NH:29][C@@H:30]3[C:38]4[C:33](=[CH:34][CH:35]=[CH:36][CH:37]=4)[CH2:32][CH2:31]3)[N:25]=[C:26]([CH3:28])[N:27]=2)[CH2:11]1)([C:4]([CH3:7])([CH3:5])[CH3:6])([CH3:2])[CH3:3]