| Identification | Back Directory | [Name]
6-BROMOISOQUINOLIN-1-YLAMINE | [CAS]
215453-26-2 | [Synonyms]
in-1-amine
6-BromoisoquinoL
6-BROMO-1-ISOQUINOLINAMINE
6-Bromoisoquinolin-1-amine
1-Amino-6-bromoisoquinoline
1-IsoquinolinaMine,6-broMo-
6-BROMOISOQUINOLIN-1-YLAMINE ISO 9001：2015 REACH
6-bromoisoquinolin-1-amine(1-amino-6-bromo isoquinoline)
6-Bromoisoquinolin-1-amine, 6-Bromo-2-azanaphthalen-1-amine | [Molecular Formula]
C9H7BrN2 | [MDL Number]
MFCD07374395
| [MOL File]
215453-26-2.mol | [Molecular Weight]
223.07 |
| Questions And Answer | Back Directory | [Synthesis]
1-Aminoisoquinoline can also be prepared from the corresponding carboxylic acid derivatives by rearrangement reaction. In this case, N-2 should be protected beforehand and then deprotected after the reaction is complete. The steps are cumbersome and the yield is low. The common preparation of 6-BROMOISOQUINOLIN-1-YLAMINE is to use 6-bromo-1-chloroisoquinoline as the starting material, which is obtained by reaction with p-methoxybenzylamine and hydrolysis [1]. The synthetic route is as follows: 
Figure 1 Synthetic route of 6-BROMOISOQUINOLIN-1-YLAMINE | [Uses]
6-Bromo-1-aminoisoquinoline has been widely used in the synthesis of several drugs, including anti-pregnancy drugs and thrombin inhibitors. |
| Chemical Properties | Back Directory | [Boiling point ]
380.7±27.0 °C(Predicted) | [density ]
1.649±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [form ]
solid | [pka]
6.92±0.38(Predicted) | [color ]
Off-white to light yellow |
| Hazard Information | Back Directory | [References]
[1] Bioorganic and Medicinal Chemistry, 2006, vol. 14, # 20, p. 6832 - 6846
[2] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 12, p. 3150 - 3155
[3] Patent: US2003/187026, 2003, A1
[4] Patent: US2003/199511, 2003, A1. Location in patent: Page/Page column 36
[5] Patent: WO2016/113271, 2016, A1. Location in patent: Page/Page column 141 |
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