{"title":"2 - {((1 s, 2 s) 1-hy-droxy-1-phenyl-propan-2-yl)(甲基)氨基}- n -乙酰胺(3-methyl-phen-yl)。","authors":"Sarvinoz Bobonazarova , Batirbay Torambetov , Dilnoza Burieva , Anvar Abdushukurov , Shakhnoza Kadirova , Rasul Ya Okmanov , Mukhriddin Yusufov","doi":"10.1107/S2414314625005784","DOIUrl":null,"url":null,"abstract":"<div><div>A chiral compound, <em>m</em>-TAP, was synthesized and its crystal structure was determined, revealing key stereochemical and supramolecular features.</div></div><div><div>The title compound, C<sub>19</sub>H<sub>24</sub>N<sub>2</sub>O<sub>2</sub> (<em>m</em>-TAP), was synthesized <em>via</em> the reaction of 2-chloro-<em>N</em>-(<em>m</em>-tolyl)acetamide with pseudoephidrine. It crystallizes in the monoclinic crystal system with a non-centrosymmetric chiral space group <em>P</em>2<sub>1</sub> (No. 4). The asymmetric unit comprises a single molecule. The dihedral angle between the phenyl rings is 89.20 (10)°. <em>m</em>-TAP contains two chiral centers at the C7 and C8 positions, both with an absolute configuration of <em>S</em>.<blockquote><div><span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (296KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></blockquote></div></div>","PeriodicalId":94324,"journal":{"name":"IUCrData","volume":"10 7","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"2-{[(1S,2S)-1-Hydroxy-1-phenylpropan-2-yl](methyl)amino}-N-(3-methylphenyl)acetamide\",\"authors\":\"Sarvinoz Bobonazarova , Batirbay Torambetov , Dilnoza Burieva , Anvar Abdushukurov , Shakhnoza Kadirova , Rasul Ya Okmanov , Mukhriddin Yusufov\",\"doi\":\"10.1107/S2414314625005784\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A chiral compound, <em>m</em>-TAP, was synthesized and its crystal structure was determined, revealing key stereochemical and supramolecular features.</div></div><div><div>The title compound, C<sub>19</sub>H<sub>24</sub>N<sub>2</sub>O<sub>2</sub> (<em>m</em>-TAP), was synthesized <em>via</em> the reaction of 2-chloro-<em>N</em>-(<em>m</em>-tolyl)acetamide with pseudoephidrine. It crystallizes in the monoclinic crystal system with a non-centrosymmetric chiral space group <em>P</em>2<sub>1</sub> (No. 4). The asymmetric unit comprises a single molecule. The dihedral angle between the phenyl rings is 89.20 (10)°. <em>m</em>-TAP contains two chiral centers at the C7 and C8 positions, both with an absolute configuration of <em>S</em>.<blockquote><div><span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (296KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></blockquote></div></div>\",\"PeriodicalId\":94324,\"journal\":{\"name\":\"IUCrData\",\"volume\":\"10 7\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IUCrData\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2414314625000665\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IUCrData","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2414314625000665","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
以2-氯- n -(间甲酰基)乙酰胺与伪麻黄碱为原料合成了标题化合物C19H24N2O2 (m-TAP)。它在单斜晶系中结晶,具有非中心对称的手性空间群P21 (No. 4)。不对称单元由单个分子组成。苯环之间的二面角为89.20(10)°。m-TAP在C7和C8位置有两个手性中心,绝对构型均为S。
A chiral compound, m-TAP, was synthesized and its crystal structure was determined, revealing key stereochemical and supramolecular features.
The title compound, C19H24N2O2 (m-TAP), was synthesized via the reaction of 2-chloro-N-(m-tolyl)acetamide with pseudoephidrine. It crystallizes in the monoclinic crystal system with a non-centrosymmetric chiral space group P21 (No. 4). The asymmetric unit comprises a single molecule. The dihedral angle between the phenyl rings is 89.20 (10)°. m-TAP contains two chiral centers at the C7 and C8 positions, both with an absolute configuration of S.