Methanol → 2-Thioadenosine

8.0 g of adenosine 1-oxide monohydrate (26.67 mmol) was refluxed in 5 ml of a 5N sodium hydroxide aqueous solution for 15 minutes. The resulting liquid was neutralized to a pH of 9.0 using Amberlite IRC-50 (H+-type) and then concentrated to a small volume to prepare 5-amino-1-β-D-ribofuranosylimidazole-4-carboxamide oxime. To this was added 200 ml of an aqueous solution containing 175 ml of methanol. The pH of the resulting solution was 9. 50 ml of carbon disulfide was further added to the solution, and the mixture was allowed to react in an autoclave at 120° C for 5 hours under autogenous pressure (about 10 Kg/cm2). The orange colored substance formed in the autoclave was removed and concentrated to dryness. The residue was dissolved in 63 ml of 2.5N aqueous ammonia, and any impurities were filtered out. A mixture of n-butanol and acetic acid (125 ml:63 ml) was added to the above filtrate to crystallize the product to obtain 8.20 g of 2-thioadenosine having a melting point of 199° C (with decomposition) in a 97% yield.

1. concentrationconcentrated to a small volume
2. customto prepare 5-amino-1-β-D-ribofuranosylimidazole-4-carboxamide oxime
3. customto react in an autoclave at 120° C for 5 hours under autogenous pressure (about 10 Kg/cm2)
4. customThe orange colored substance formed in the autoclave
5. customwas removed
6. concentrationconcentrated to dryness
7. dissolutionThe residue was dissolved in 63 ml of 2.5N aqueous ammonia
8. filtrationany impurities were filtered out
9. additionA mixture of n-butanol and acetic acid (125 ml:63 ml)
10. additionwas added to the above filtrate
11. customto crystallize the product

ORD 기록

ord-b3a4c919e3dc4f889739101643e5dc92

출처 데이터셋

uspto-grants-1976_11

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US03989682