반응 #2446088

ord-1027e35c3241449f807b23f72181631a

반응 방정식

CC(CN(C)C1CCCCC1)OC(=O)c1ccc(C(C)C)cc1
1-(cyclohexyl(methyl)amino)propan-2-yl 4-isopropylbenzoate
CI
methyl iodide
CC(C[N+](C)(C)C1CCCCC1)OC(=O)c1ccc(C(C)C)cc1.[I-]
N-[2-((4-Isopropylbenzoyl)oxy)propyl]-N,N-dimethylcyclohexanaminium iodide

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The resultant reaction mixture
  2. 2
    기타The solvent was evaporated
  3. 3
    기타the crude product was purified by column chromatography
  4. 4
    기타The product isolated
  5. 5
    기타was re-crystallized from methanol/ether
  6. 6
    기타99.65% (200 nm), RT 3.09 min

실험 절차

To a solution of 1-(cyclohexyl(methyl)amino)propan-2-yl 4-isopropylbenzoate (0.5 g, 1.57 mmol) in DCE (5 mL, methyl iodide (0.2 mL, 3.15 mmol) was added. The resultant reaction mixture was stirred at rt for 16 hours. The solvent was evaporated, and the crude product was purified by column chromatography. The product isolated was re-crystallized from methanol/ether. Yield: 134.9 mg (18.65%). 1H NMR (400 MHz, DMSO-d6) δ 7.94-7.92 (d, J=8 Hz, 2 H), 7.43-7.41 (d, J=8 Hz, 2 H), 5.54-5.50 (m, 1 H), 3.95-3.89 (m, 1 H), 3.61-3.58 (d, J=14 Hz, 1 H), 3.40-3.34 (m, 1 H), 3.03-2.95 (m, 7 H), 2.22-2.20 (d, J=11 Hz, 1 H), 2.10-2.07 (d, J=11 Hz, 1 H), 1.86-1.83 (m, 2 H), 1.57-1.43 (m, 3 H), 1.36-1.35 (d, J=6 Hz, 3 H), 1.16-1.11 (m, 9 H). LCMS: m/z=331.8 [M+], RT=3.08 min (Column: Y, Program: P1). UPLC: 99.65% (200 nm), RT 3.09 min (Mobile phase: A. ACN, B. 0.05% HCOOH in water, Column: Gemini® NX C18 (50*4.6 mm) 3μ.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08685418B2uspto-grants-2014_04