HRID503644

反应详情

EQUATION

反应方程式

HRID 503644 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

In a 20 mL sealed tube was dissolved tert-butyl 4-(4-(4-(7-methoxy-1,5-naphthyridin-4-ylthio)phenylamino)phthalazin-1-yl)-5,6-dihydropyridine-1(2H)-carboxylate (0.200 g, 0.337 mmol) in DCM (1.00 mL). To the mixture was added TFA (0.130 mL, 1.69 mmol). The mixture was stirred at 50° C. for 3 hours, then cooled to RT and concentrated. The crude material was purified on an Isco silica gel chromatography using 0-100% CH2Cl2:MeOH:NH4OH (90:10:1)/CH2Cl2. The product fractions were concentrated to yield N-(4-(7-methoxy-1,5-naphthyridin-4-ylthio)phenyl)-4-(1,2,3,6-tetrahydropyridin-4-yl)phthalazin-1-amine as a light yellow solid. MS: [N+H]=493.0; Calc'd 492.6 for C28H24N6OS.

WORKUP

后处理

  1. customIn a 20 mL sealed tube
  2. temperaturecooled to RT
  3. concentrationconcentrated
  4. customThe crude material was purified on an Isco silica gel chromatography
  5. concentrationThe product fractions were concentrated