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HRID 260143作成日:2026年10月27日

Ammonium Sulfate → 4-Amino-2-phenyl-8-[2-deoxy-3,5-di-O-(4-chlorobenzoyl)-beta-D-ribofuranosyl]-pteridine-7-one

https://huagongshe.com/reaction/260143

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium SulfateHCID 6097028—
反応物alpha-D-erythro-Pentofuranosyl chloride, 2-deoxy-, 3,5-bis(4-chlorobenzoate)HCID 9845541—
反応物4-Amino-2-phenyl-pteridine-7-oneHCID 54402511—
触媒Silver perchlorateHCID 24562—
溶媒DichloromethaneHCID 6344—
溶媒HexamethyldisilazaneHCID 13838—
生成物4-Amino-2-phenyl-8-[2-deoxy-3,5-di-O-(4-chlorobenzoyl)-beta-D-ribofuranosyl]-pteridine-7-oneHCID 15403909—

反応手順

A mixture of 1.0 g (4.2 mmol) of 4-amino-2-phenyl-pteridine-7-one (3) and a few crystals of ammonium sulfate was heated in 100 mL of hexamethyldisilazane (HMDS) under reflux for 4 hours. After cooling the excess HMDS was distilled off in vacuum and the residue dissolved in 100 mL of dry toluene. To the mixture was added 2.17 g (4.6 mmol) of 2-deoxy-3,5-di-O-(4-chlorobenzoyl)-α-D-ribofuranosyl chloride (made as in Example 3, step (a) for the toluyl derivative) and 0.476 g (2.3 mmol) of silver perchlorate. The solution was then stirred under anhydrous conditions for 24 hours at room temperature and then diluted with 200 mL of CH2Cl2. The resulting AgCl precipitate was filtered off through silica and then the flitrate was treated with 100 mL of a saturated aqueous solution of sodium bicarbonate followed by 100 mL of a saturated aqueous solution of NaCl. The organic layer was dried over Na2SO4, filtered and then the flitrate evaporated.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05525711
出典データセットuspto-grants-1996_06
ORD IDord-709d959ee68d47eb90ce4ec250c5f310
出典メモuspto-grants-1996_06