876343-09-8 (7-(苯磺酰基)-4-氯-6-碘-吡咯并[2,3-D]嘧啶,7-(benzenesulfonyl)-4-chloro-6-iodo-7H-pyrrolo[2,3-d]pyrimidine)

CAS号:
876343-09-8
中文名称:
7-(苯磺酰基)-4-氯-6-碘-吡咯并[2,3-D]嘧啶
英文名称:
7-(benzenesulfonyl)-4-chloro-6-iodo-7H-pyrrolo[2,3-d]pyrimidine
分子式:
C12H7ClIN3O2S
分子量:
419.625352144241

7-(苯磺酰基)-4-氯-6-碘-吡咯并[2,3-D]嘧啶(876343-09-8)名称与标识符

名称

英文别名:
4-Chloro-6-iodo-7-phenylsulfonyl-7H-pyrrolo[2,3-d]pyrimidine;4-Chloro-6-iodo-7-phenylsulfonyl-7H-pyrrolo(2,3-d)pyrimidine;7-(Benzenesulfonyl)-4-chloro-6-iodo-pyrrolo[2,3-d]pyrimidine;4-chloro-6-iodo-7-(phenylsulfonyl)-7H-pyrrolo[2,3-d]pyrimidine;C-8572;Y4440;7-(benzenesulfonyl)-4-chloro-6-iodo-7H-pyrrolo[2,3-d]pyrimidine;7-(benzenesulfonyl)-4-chloro-6-iodopyrrolo[2,3-d]pyrimidine;C12H7ClIN3O2S;PEVCDMDOTQHPPL-UHFFFAOYSA-N;PB11200;4-Chloro-6-iodo-7-(phenylsulfonyl)-7H-pyrrolo[2,3-d]pyrimidine (ACI);7-(Phenylsulfonyl)-4-chloro-6-iodopyrrolo[2,3-d]pyrimidine;

标识符

MDL:
MFCD17015878
InChIKey:
PEVCDMDOTQHPPL-UHFFFAOYSA-N
Inchi:
1S/C12H7ClIN3O2S/c13-11-9-6-10(14)17(12(9)16-7-15-11)20(18,19)8-4-2-1-3-5-8/h1-7H
SMILES:
O=S(N1C2C(=C(N=CN=2)Cl)C=C1I)(C1C=CC=CC=1)=O

7-(苯磺酰基)-4-氯-6-碘-吡咯并[2,3-D]嘧啶(876343-09-8)物化性质

实验特性

  • LogP : 4.00710
  • PSA : 73.23000

计算特性

  • 精确分子量 : 418.89900
  • 氢键供体数量 : 0
  • 氢键受体数量 : 4
  • 可旋转化学键数量 : 2
  • 重原子数量 : 20
  • 复杂度 : 452
  • 拓扑分子极性表面积 : 73.2

7-(苯磺酰基)-4-氯-6-碘-吡咯并[2,3-D]嘧啶(876343-09-8)推荐厂家 更多厂家(14)

7-(苯磺酰基)-4-氯-6-碘-吡咯并[2,3-D]嘧啶(876343-09-8)合成路线

合成路线:1 步
反应条件:
参考文献:
Combating Drug-Resistant Mutants of Anaplastic Lymphoma Kinase with Potent and Selective Type-I1/2 Inhibitors by Stabilizing Unique DFG-Shifted Loop Conformation
Pan, Peichen; et al, ACS Central Science, 2017, 3(11), 1208-1220
合成路线:1 步
反应条件:
参考文献:
Novel hinge-binding motifs for janus kinase 3 inhibitors: a comprehensive structure-activity relationship study on tofacitinib bioisosteres
Gehringer, Matthias; et al, ChemMedChem, 2014, 9(11), 2516-2527
合成路线:2 步
反应条件:
参考文献:
Novel hinge-binding motifs for janus kinase 3 inhibitors: a comprehensive structure-activity relationship study on tofacitinib bioisosteres
Gehringer, Matthias; et al, ChemMedChem, 2014, 9(11), 2516-2527
合成路线:3 步
反应条件:
参考文献:
Identification of new 4-N-substituted 6-aryl-7H-pyrrolo[2,3-d]pyrimidine-4-amines as highly potent EGFR-TK inhibitors with Src-family activity
Kaspersen, Svein Jacob; et al, European Journal of Pharmaceutical Sciences, 2014, 59, 69-82
合成路线:1 步
反应条件:
参考文献:
Balancing potency, metabolic stability and permeability in pyrrolopyrimidine-based EGFR inhibitors
Han, Jin; et al, European Journal of Medicinal Chemistry, 2016, 124, 583-607