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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 260143생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium SulfateHCID 6097028—
반응물alpha-D-erythro-Pentofuranosyl chloride, 2-deoxy-, 3,5-bis(4-chlorobenzoate)HCID 9845541—
반응물4-Amino-2-phenyl-pteridine-7-oneHCID 54402511—
촉매Silver perchlorateHCID 24562—
용매DichloromethaneHCID 6344—
용매HexamethyldisilazaneHCID 13838—
생성물4-Amino-2-phenyl-8-[2-deoxy-3,5-di-O-(4-chlorobenzoyl)-beta-D-ribofuranosyl]-pteridine-7-oneHCID 15403909—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05525711
출처 데이터셋uspto-grants-1996_06
ORD IDord-709d959ee68d47eb90ce4ec250c5f310
출처 메모uspto-grants-1996_06