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【结 构 式】 
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【分子编号】30048 【品名】N-[9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-2-[(3,3,3-trifluoropropyl)sulfanyl]-9H-purin-6-yl]-N-[2-(methylsulfanyl)ethyl]acetamide 【CA登记号】 |
【 分 子 式 】C18H24F3N5O5S2 【 分 子 量 】511.5464696 【元素组成】C 42.26% H 4.73% F 11.14% N 13.69% O 15.64% S 12.54% |
合成路线1
该中间体在本合成路线中的序号：(VI)Alkylation of mercaptopurine (I) with 3-chloro-1,1,1-trifluoropropane (II) in the presence of NaH gave thioether (III). After protection of the amino group of (III) as the acetamide (IV) by means of Ac2O and NaOAc, N-alkylation with 2-(methylthio)ethyl iodide (V) yielded (VI), which was deacetylated by hydrolysis with NaOH in refluxing MeOH. Subsequent treatment with POCl3 produced the intermediate phosphoryl chloride (VIII). Then, condensation of this acid chloride with dichloromethylene bisphosphonic acid (IX) in the presence of tributylamine in triethyl phosphate yielded the title compound, which was isolated as the tetrasodium salt. Alternatively, hydrolysis of acid chloride (VIII) in the presence of ammonium bicarbonate gave phosphate salt (X), which was treated with carbonyldiimidazole, and the activated intermediate (XI) was then condensed with bisphosphonate (IX) to furnish the target compound.
| 【1】 Cage, P.A.; Bailey, A.; Kindon, N.D.; et al.; SAR studies on AR-C 69931MX, a potent and selective intravenous anti-aggregatory/anti-thrombotic agent with a novel mechanism of action. 15th European Federation for Medicinal Chemistry International Symposium on Medicinal Chemistry (Sept 6 1998, Edinburgh) 1998, Abst P.281. |
| 【2】 Ingall, A.H.; Cage, P.A.; Kindon, N.D. (Celltech Medeva plc); N-Alkyl-2-substd. ATP analogues. EP 0683789; JP 1996506335; US 5721219; WO 9418216 . |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (I) | 22306 | (2R,3R,4S,5R)-2-(6-amino-2-sulfanyl-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydro-3,4-furandiol | C10H13N5O4S | 详情 | 详情 | |
| (II) | 22307 | 3-chloro-1,1,1-trifluoropropane | C3H4ClF3 | 详情 | 详情 | |
| (III) | 22308 | (2R,3R,4S,5R)-2-[6-amino-2-[(3,3,3-trifluoropropyl)sulfanyl]-9H-purin-9-yl]-5-(hydroxymethyl)tetrahydro-3,4-furandiol | C13H16F3N5O4S | 详情 | 详情 | |
| (IV) | 30047 | N-[9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-2-[(3,3,3-trifluoropropyl)sulfanyl]-9H-purin-6-yl]acetamide | C15H18F3N5O5S | 详情 | 详情 | |
| (V) | 22310 | 1-iodo-2-(methylsulfanyl)ethane; 2-iodoethyl methyl sulfide | C3H7IS | 详情 | 详情 | |
| (VI) | 30048 | N-[9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydro-2-furanyl]-2-[(3,3,3-trifluoropropyl)sulfanyl]-9H-purin-6-yl]-N-[2-(methylsulfanyl)ethyl]acetamide | C18H24F3N5O5S2 | 详情 | 详情 | |
| (VII) | 22312 | (2R,3S,4R,5R)-2-(hydroxymethyl)-5-[6-[[2-(methylsulfanyl)ethyl]amino]-2-[(3,3,3-trifluoropropyl)sulfanyl]-9H-purin-9-yl]tetrahydro-3,4-furandiol | C16H22F3N5O4S2 | 详情 | 详情 | |
| (VIII) | 30049 | 5'-O-(Dichlorophosphoryl)-N6-[2-(methylsulfanyl)ethyl]-2-(3,3,3-trifluoropropylsulfanyl)adenosine | C16H21Cl2F3N5O5PS2 | 详情 | 详情 | |
| (IX) | 22305 | dichloro(phosphono)methylphosphonic acid | CH4Cl2O6P2 | 详情 | 详情 | |
| (X) | 30050 | 5'-O-(Dihydroxyphosphoryl)-N6-[2-(methylsulfanyl)ethyl]-2-(3,3,3-trifluoropropylsulfanyl)adenosine monoammonium salt | C16H26F3N6O7PS2 | 详情 | 详情 | |
| (XI) | 22314 | ((2R,3S,4R,5R)-3,4-dihydroxy-5-[6-[[2-(methylsulfanyl)ethyl]amino]-2-[(3,3,3-trifluoropropyl)sulfanyl]-9H-purin-9-yl]tetrahydro-2-furanyl)methyl hydrogen 1H-imidazol-1-ylphosphonate | C19H25F3N7O6PS2 | 详情 | 详情 |