تفاعل #1256736
ord-def81f503ff74d67990aadde8e8e6be9
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.STIRRINGstirred for 18 hrs
- 2ترشيحfiltered
- 3أخرىThe solvent of the filtrate was partially removed in vacuo
- 4workup.ADDITIONthe impure solution was added dropwise to cold diethyl ether
- 5ترشيحThe resulting precipitate (2) was filtered
- 6أخرىdried
- 7أخرىfollowed by acidolytic removal (treating Boc-Val-ACV with trifluoroacetic acid (TFA) for 30 min at 0° C.) of the Boc protecting group
الإجراء التجريبي
A mixture of Boc-Val and dicyclohexyl carbodiimide (DCC) in dimethylformamide (DMF) in a ratio of 1:2 DCC/Boc-Val was stirred for 1 hr at 0° C. under nitrogen atmosphere. A solution of acyclovir (1) and 4-N,N(dimethylamino)pyridine (DMAP) was added to the reaction mixture, stirred for 18 hrs and then filtered. The solvent of the filtrate was partially removed in vacuo and the impure solution was added dropwise to cold diethyl ether. The resulting precipitate (2) was filtered and dried, followed by acidolytic removal (treating Boc-Val-ACV with trifluoroacetic acid (TFA) for 30 min at 0° C.) of the Boc protecting group to yield Val-ACV (3). Compound (3) was neutralized by triethylamine (TEA) and treated with the amino acid anhydride of Boc-Val for about 5 hrs. The solvent was removed from the reaction mixture in vacuo and the reaction mixture was added dropwise to the cold diethyl ether. The resulting precipitate (4) was filtered, dried and the Boc group was deprotected (acidolytic removal) to yield the desired dipeptide ester of acyclovir Val-Val-ACV (5).