Macrocyclic derivatives as protein kinase inhibitors and their preparation and use
A kind of use and drug technology, applied in the field of disease drugs, macrocyclic derivatives and their preparation, can solve the problems of high incidence of adverse reactions, low bioavailability, large dosage, etc., and achieve good clinical application and medicine The effect of use
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0057] Embodiment 1: compound shown in synthetic formula I-1
[0058] synthetic route:
[0059]
[0060] Preparation:
[0061] Step 1: Synthesis of Compound 1B
[0062] In the first reaction vessel, to a solution of cooled (0 °C) water (3.5 mL) was added SOC1 2 (0.642 mL, 1.64 g / mL, 8.84 mmol) and allowed to warm to room temperature and stir for 1 hour. Then cuprous chloride (19mg, 0.20mmol) was added, and the solution was cooled to -5°C to obtain the first mixed solution. In a second reaction vessel, dissolve in HCl (1.97 mL, 37% in H 2 O, 1.18g / mL, 23.6mmol) solution was added compound 1A (500mg, 2.5mmol) (synthetic reference patent WO2015050989A1), and cooled to -5 ° C, then sodium nitrite (149mg, 2.16mmol) in water ( 1 mL) solution was added thereto to obtain a second mixed solution. Then the second mixed solution was added dropwise to the first mixed solution, and kept at -5°C by cooling. After the dropwise addition was completed, the third mixed solution was ob...
Embodiment 2
[0083] Embodiment 2: compound shown in synthetic formula I-2
[0084]
[0085] The compound of Example 2 was synthesized with reference to the operation steps of Example 1, but methylamine hydrochloride was replaced with ethylamine hydrochloride in the second step.
[0086] MS m / z(ESI):471[M+1]
[0087] 1 H NMR (400MHz, CDCl 3 )δ7.84(d, 1H, J=2.0Hz), 7.32(dd, 1H, J=9.6, 2.4Hz), 7.23(dd, 1H, J=8.0, 5.2Hz), 7.01(dt, 1H, J =8.4,2.4Hz),6.86(d,1H,J=1.6Hz),5.71-5.75(m,1H),4.85(s,2H),4.08(s,3H),3.24(m,2H),1.78 (d, 3H, J=6.4Hz), 1.19 (t, 3H, J=6.90Hz).
Embodiment 3
[0088] Embodiment 3: compound shown in synthetic formula I-3
[0089]
[0090] The compound of Example 3 was synthesized with reference to the operation steps of Example 1, but in the first step, it was replaced with 3-amino-4-bromo-1-ethyl-1H-pyrazole-5-carbonitrile (synthetic reference patent WO2015050989A1) 3-Amino-4-bromo-1-methyl-1H-pyrazole-5-carbonitrile was dropped.
[0091] MS m / z(ESI):471[M+1]
[0092] 1 H NMR (400MHz, CDCl 3 )δ7.85 (d, 1H, J = 2.0Hz), 7.31 (dd, 1H, J = 9.6, 2.4Hz), 7.22 (dd, 1H, J = 8.4, 5.6Hz), 6.98 (dt, 1H, J =8.0,2.8Hz),6.87(d,1H,J=1.2Hz),5.71-5.75(m,1H),4.85(s,2H),4.12(q,2H,J=7.2Hz),3.24(s , 3H), 1.78 (d, 3H, J=6.0Hz), 1.28 (t, 3H, J=7.1Hz).
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


