Catalytic Activity of 1,3-Dibromo-5,5-dimethylhydantoin (DBH) in the One-Pot Transformation ofN-Arylglycines toN-Arylsydnones in the Presence of NaNO2/Ac2O under Neutral Conditions: Subsequent Bromination of these Sydnones to their 4-Bromo Derivatives
Microwave-assisted Synthesis of N-Arylglycines: Improvement of Sydnone Synthesis
摘要:
Reactions of anilines with ethyl bromoacetate under microwave irradiation have afforded N-arylglycines that are subsequently converted to their N-nitroso derivatives with a combination of silica chloride or periodic acid, wet SiO2 and sodium nitrite in CH2Cl2 with satisfactory yields. In the final step, the use of 1,3-dibromo-5,5-dimethylhydantoin (DBH) as a new and effective reagent for dehydration of N-nitroso-N-arylglycines to sydnones was successfully examined.
One-Pot Conversion of N-Arylglycines to Sydnones Efficiently Promoted by Bis-chlorine-1,4-diazabicyclo[2.2.2]octane Complex (Cl2-DABCO) in the Presence of NaNO2/Ac2O under Neutral Conditions
Bis-chlorine-1,4-diazabicyclo[2.2.2]octane complex, (Cl 2 -DABCO), has been found as an active chlorine complex for effective one-potconversion of various N-arylglycines to sydnones in high yields (85-95%) under mild and neutral condition.
N,N,N’,N’-Tetrabromobenzene-1,3-disolfonamide (TBBDS) as an Efficient Promoter for One-Pot Conversion of N-Arylglycines to Sydnones in the Presence of NaNO2/Ac2O under Neutral Conditions
N,N,N',N'-Tetrabromobenzene-1,3-disolfonamide (TBBDS)-promoted one-potconversion of various N-arylglycines to sydnones using a combination of NaNO 2 and Ac 2 O has been achieved efficiently through N-nitrosation followed by cyclization in high yields (85-95%) under mild and neutralconditions.
N,N,N',N'-四溴苯-1,3-二磺酰胺 (TBBDS) - 使用 NaNO 2 和 Ac 2 O 的组合促进了各种 N-芳基甘氨酸到 sydnones 的一锅转化,通过 N-亚硝化,然后在温和和中性条件下以高产率 (85-95%) 环化。
N-Bromosuccinimide (NBS) as Promoter for Acylation of Sydnones in the Presence Acetic Anhydride under Neutral Conditions
Various 4 - acetyl sydnones (2) can be prepared by reaction of the corresponding 3-aryl sydnones (1) with aceticanhydride at ∼110 °C promoted by N-Bromosuccinimide (NBS) as an effective reagent for acylation of sydnones underneutralconditions in satisfactory yields.
1,3-Dibromo-5,5-dimethylhydantoin (DBH) as an efficient promoter for acetylation of 3-arylsydnones in the presence of acetic anhydride under neutral conditions
1,3-Dibromo-5,5-dimethylhydantoin (DBH) has been found to efficiently promote the conversion of various 3-arylsydnones to their 4-acetyl congeners in the presence of aceticanhydrideunderneutralconditions in satisfactory yields.