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164148-92-9, The synthetic route of 164148-92-9 has been constantly updated, and we look forward to future research findings.

164148-92-9, tert-Butyl 6-amino-3,4-dihydroisoquinoline-2(1H)-carboxylate is a isoquinoline compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

tert-Butyl 6-amino-3,4-dihydroisoquinoline-2(lH)-carboxylate (99.3 mg,0.4 mmol) and mesylate 27c (123 mg, 0.4 mmol) were dissolved in MeCN (1 mL). Cs2CO3 (261 mg, 0.8 mmol) was added and the mixture was stirred at 9O0C overnight. The mixture was then diluted with MeCN and filtered. The filtrate was purified by reverse-phase HPLC to yield the title compound (Example 29). 1H-NMR (400 MHz, CD3CN) delta = 7.04 (d, J = 8.4 Hz, IH), 6.81 (dd, J = 8.4, 2.4 Hz, IH), 6.76 (s, IH), 4.83 (septet, J = 6.4 Hz, IH), 4.47 (s, 2H), 4.04 (br. d, J = 13.2 Hz, 2H), 3.58 (t, / = 6.0 Hz, 2H), 3.15 (t, J = 7.6 Hz, 2H), 2.76 (t, J = 6.0 Hz, 2H), 2.76-2.68 (m, 2H), 1.69-1.61 (m, 4H), 1.47 (s, 9H), 1.47-1.40 (m, IH), 1.34-1.28 (m, 2H), 1.21 (d, J = 6.4 Hz, 6H), 1.02 (ddd, J = 12.8, 12.4, 4.0 Hz, 2H); MS calcd. for [M+2H-Boc]+ C21H34N3O2: 360.2; found: 360.1.

164148-92-9, The synthetic route of 164148-92-9 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; IRM LLC; WO2008/97428; (2008); A2;,
Isoquinoline – Wikipedia
Isoquinoline | C9H7N – PubChem