反応 #1704434
ord-9d98d595517e4862b82eace92a89943c
反応方程式
product
2-(4-((2-Amino-4-chloro-6-methylpyrimidin-5-yl)methyl)phenyl)acetonitrile
(S)-3-aminohexan-1-ol
butan-1-ol
KOH
→
subtitle compound
(S)-2-(4-((2-Amino-4-(1-hydroxyhexan-3-ylamino)-6-methylpyrimidin-5-yl)methyl)phenyl)acetic acid
反応物
試薬
なし
反応条件
温度
100°CELSIUS
詳細条件
See reaction.notes.procedure_details.
後処理
- 1その他was sealed into a microwave tube
- 2その他was performed in the CEM Microwave, at 160° C.
- 3温度The mixture was cooled
- 4その他the solvent evaporated under reduced pressure
- 5その他The residue was purified by RPHPLC
実験手順
A mixture of the product of example 81 step (iii) (0.4 g) and (S)-3-aminohexan-1-ol (0.5 g) in butan-1-ol (3 mL) was sealed into a microwave tube. The reaction was performed in the CEM Microwave, at 160° C. and 100 W for 1.5 h. Aq. 5M KOH (iml) was added and the mixture heated at 100° C. for 48 h. The mixture was cooled and the solvent evaporated under reduced pressure. The residue was purified by RPHPLC to give the subtitle compound, 174 mg.