Methyl 4-amino-2-chloropyrimidine-5-carboxylate
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چکیده
منابع مشابه
Ethyl 5-(4-Bromophenyl)-4-methyl-1H-pyrrole- 2-carboxylate
This note describes a sequence converting an oxime-substituted pyrrolidine into a trisubstituted pyrrole structure. The synthetic route is based on a double chlorination of the pyrrolidine substrate followed by the base induced formation of both an imine and a nitrile oxide functionality. The latter reacts with an immobilized thiourea to yield an isothiocyanate which upon elimination generates ...
متن کاملMethyl 4-amino-2-chloropyrimidine-5-carboxylate
In the title compound, C6H6ClN3O2, all non-H atoms are approximately coplanar [maximum deviation = 0.012 (4) Å]; an intra-molecular N-H⋯O hydrogen bond occurs between the amino group and the carbonyl group. In the crystal, mol-ecules are linked by N-H⋯N hydrogen bonds into supra-molecular chains propagated along [101].
متن کاملEthyl 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-5-methyl-1H-1,2,3-triazole-4-carboxylate
In the title compound, C(10)H(11)ClN(4)O(2)S, the triazole ring carries methyl and ethoxy-carbonyl groups and is bound via a methyl-ene bridge to a chloro-thia-zole unit. There is also evidence for significant electron delocalization in the triazolyl system. Intra- and inter-molecular C-H⋯O hydrogen bonds together with strong π-π stacking inter-actions [centroid-centroid distance 3.620 (1) Å] s...
متن کاملCrystal structure of methyl 5-acetamido-2-t-butyl-2-methyl-1,3-benzodioxole-4-carboxylate.
1,3-benzodioxle-4-carboxylic acid] was designed as a novel class of chiral fluorometric agents.1 The chiral agent and the analogues have been conveniently applied to enantiomer analyses of various bio-molecules using HPLC and circular dichroism.2 We recently extended the molecular design of (S)TBMB carboxylic acid to chiral nitrobenzoic acids possessing the asymmetric 1,3-benzodioxole.3 The chi...
متن کاملAcetylation of methyl 5-amino-1H-[1,2,4]triazole-3-carboxylate.
Acetylation with acetic anhydride of methyl 5-amino-1H-[1,2,4]triazole-3-carboxylate, one of the hetareneamino acids, was studied using HPLC, H NMR, FTIR and GC-MS. The compound has a significantly decreased susceptibility to acetylation compared to 5-amino-1H-[1,2,4]triazole itself. Two isomeric diacetylated products were found.
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ژورنال
عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online
سال: 2014
ISSN: 1600-5368
DOI: 10.1107/s1600536814016080