Hydrochloric Acid → 8-Quinolinamine,1,2,3,4-tetrahydro-1-methyl-(9CI)

Anhydrous HCl (gas) was bubbled through a stirred solution of 1-methyl-8-(N-tert-butoxycarbonylamino)-1,2,3,4-tetrahydroquinoline (0.83 g, 3.16 mmol) in methanol (30 mL), at room temperature, for 10 minutes. The resultant solution was stirred at room temperature for 1 hour then concentrated under reduced pressure. The residue was partitioned between CH2Cl2 (50 mL) and aqueous NaOH (10 N, 10 mL). The phases were separated and the aqueous phase was extracted with CH2Cl2 (3×10 mL). The combined organic extracts were dried (Na2SO4) and concentrated to afford 0.468 g (88%) of 1-methyl-8-amino-1,2,3,4-tetrahydroquinoline as a white solid. 1H NMR (CDCl3) δ 1.83–1.91 (m, 2H), 2.69 (s, 3H), 2.78 (t, 2H, J=6.6 Hz), 3.07–3.11 (m, 2H), 3.84 (br s, 2H, NH2), 6.52 (d, 1H, J=7.5 Hz), 6.56 (d, 1H, J=7.5 Hz), 6.81 (dd, 1H, J=7.5, 7.5 Hz).

1. concentrationthen concentrated under reduced pressure
2. customThe residue was partitioned between CH2Cl2 (50 mL) and aqueous NaOH (10 N, 10 mL)
3. customThe phases were separated
4. extractionthe aqueous phase was extracted with CH2Cl2 (3×10 mL)
5. dry with materialThe combined organic extracts were dried (Na2SO4)
6. concentrationconcentrated

ORD record

ord-cc0538a894b9427eb1b4f3843e440377

Source dataset

uspto-grants-2007_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07183273B2