{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,1,12]],"date-time":"2025-01-12T05:18:04Z","timestamp":1736659084600,"version":"3.32.0"},"reference-count":11,"publisher":"International Union of Crystallography (IUCr)","issue":"6","license":[{"start":{"date-parts":[[2009,5,20]],"date-time":"2009-05-20T00:00:00Z","timestamp":1242777600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/2.0\/uk\/legalcode"},{"start":{"date-parts":[[2009,5,20]],"date-time":"2009-05-20T00:00:00Z","timestamp":1242777600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/2.0\/uk\/legalcode"}],"content-domain":{"domain":["iucr.org","wiley.com","iucrj.org"],"crossmark-restriction":true},"short-container-title":["Acta Crystallogr E Struct Rep Online","Acta Crystallogr E","Acta Cryst E","Acta Cryst E Struct Rep Online","Acta Cryst Sect E","Acta Cryst Sect E Struct Rep Online","Acta Crystallogr Sect E","Acta Crystallogr Sect E Struct Rep Online"],"published-print":{"date-parts":[[2009,6,1]]},"abstract":"<jats:p>In the title compound, C<jats:sub>18<\/jats:sub>H<jats:sub>15<\/jats:sub>N<jats:sub>3<\/jats:sub>O<jats:sub>3<\/jats:sub>\u00b70.5CH<jats:sub>2<\/jats:sub>Cl<jats:sub>2<\/jats:sub>, the fused ring benzofuro[2,3-<jats:italic>d<\/jats:italic>]pyrimidine system is essentially planar [maximum deviation 0.029\u2005(1)\u2005\u00c5]. The planes of the pyrimidinone and phenyl rings are nearly perpendicular [dihedral angle = 87.50\u2005(14)\u00b0]. The packing of the molecules in the crystal structure is governed mainly by intermolecular O\u2014H...O and N\u2014H...O hydrogen-bonding interactions and intermolecular \u03c0\u2013\u03c0 interactions between benzofuro[3,2-<jats:italic>d<\/jats:italic>]pyrimidine units [the interplanar distances are<jats:italic>ca<\/jats:italic>3.4 and 3.5\u2005\u00c5, and the distances between adjacent ring centroids are in the range 3.64\u2005(1)\u20133.76\u2005(1)\u2005\u00c5]. The dichloromethane solvent molecule lies on a special position.<\/jats:p>","DOI":"10.1107\/s1600536809017814","type":"journal-article","created":{"date-parts":[[2009,5,20]],"date-time":"2009-05-20T07:15:13Z","timestamp":1242803713000},"page":"o1330-o1330","update-policy":"https:\/\/doi.org\/10.1107\/cm_01","source":"Crossref","is-referenced-by-count":0,"title":["2-(2-Hydroxyethylamino)-3-phenyl-1-benzofuro[3,2-<i>d<\/i>]pyrimidin-4(3<i>H<\/i>)-one dichloromethane hemisolvate"],"prefix":"10.1107","volume":"65","author":[{"given":"Zheng-Hong","family":"Zhang","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Xiao-Ling","family":"Liu","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Long-Ju","family":"Chen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"329","published-online":{"date-parts":[[2009,5,20]]},"reference":[{"key":"at2780_bb1","first-page":"187","volume":"80","author":"Bodke","year":"2003","journal-title":"J. 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