반응 #3797
ord-e25215ee60094b58ac72c52a0aebb599
반응 방정식
2-[2-[2-(1-tert-butoxycarbonyl-3-methyl- butylcarbamoyl)-4-methoxy-phenyldisulfanyl]-5-methoxybenzoylamino]-4-methyl-pentanoic acid tert-butyl ester
2-[2-[2-(1-tert-Butoxycarbonyl-3-methylbutylcarbamoyl)-4-methoxy- phenyldisulfanyl]-5-methoxybenzoylamino]-4-methyl-pentanoic acid tert-butyl ester
trifluoroacetic acid
anisole
→
반응물
2-[2-[2-(1-tert-butoxycarbonyl-3-methyl- butylcarbamoyl)-4-methoxy-phenyldisulfanyl]-5-methoxybenzoylamino]-4-methyl-pentanoic acid tert-butyl ester
2-[2-[2-(1-tert-Butoxycarbonyl-3-methylbutylcarbamoyl)-4-methoxy- phenyldisulfanyl]-5-methoxybenzoylamino]-4-methyl-pentanoic acid tert-butyl ester
trifluoroacetic acid
anisole
시약
없음
반응 조건
상세 조건
See reaction.notes.procedure_details.
후처리
- 1기타This compound was prepared
- 2기타The crude product was recrystallized from methanol/water
실험 절차
This compound was prepared according to the procedure described in Example 50 using [S-(R*,R*)]-2-[2-[2-(1-tert-butoxycarbonyl-3-methyl- butylcarbamoyl)-4-methoxy-phenyldisulfanyl]-5-methoxybenzoylamino]-4-methyl-pentanoic acid tert-butyl ester (2.4 g, 3.4 mmol) from Example 31, 25 mL dichloromethane, 25 mL trifluoroacetic acid and 2.5 mL anisole. The crude product was recrystallized from methanol/water to afford 0.7 g of the title compound, mp 168°-169° C.