Trifluoroacetic acid → HCID 59605256, compound

HRID 1945573Notes

Reaction equation

HRID 1945573 reaction equation
FC(F)(F)C(O)=O.C(OC([N:15]1[CH2:18][CH:17]([CH2:19][N:20]([CH3:25])[CH:21]2[CH2:24][O:23][CH2:22]2)[CH2:16]1)=O)(C)(C)C>ClCCl>[NH:15]1[CH2:16][CH:17]([CH2:19][N:20]([CH3:25])[CH:21]2[CH2:22][O:23][CH2:24]2)[CH2:18]1

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 59606132HCID 59606132, compound

Product 1

HCID 59605256HCID 59605256, compoundYield 90%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

Trifluoroacetic acid (3 mL) was added to a solution of 3-[(methyl(oxetan-3-yl)amino)methyl]azetidine-1-carboxylic acid tert-butyl ester (330 mg, 1.29 mmol) in dichloromethane (12 mL) The resulting reaction mixture was stirred at RT for 1.5 h. The solvents were reduced in vacuo. The resulting residue was loaded onto an Isolute® SCX-2 cartridge (5 g). The cartridge was washed with DCM/MeOH, the desired product was subsequently eluted using a mixture of 2M NH3 in MeOH and DCM to afford (Azetidin-3-ylmethyl)methyl(oxetan-3-yl)amine as colourless oil (180 mg, 90%). 1H NMR (400 MHz, CDCl3): δ 4.64 (2 H, t, J=6.59 Hz), 4.57 (2 H, t, J=6.31 Hz), 3.72 (2 H, t, J=7.87 Hz), 3.58-3.49 (1 H, m), 3.37 (2 H, t, J=7.22 Hz), 2.92-2.82 (1 H, m), 2.44 (3 H, m), 2.06 (3 H, s)

Workup

  1. customThe resulting reaction mixture
  2. washThe cartridge was washed with DCM/MeOH
  3. washthe desired product was subsequently eluted
  4. additiona mixture of 2M NH3 in MeOH and DCM

Sources & evidence

ORD record
ord-e81355a819f24ae9a15c04555e66ac2d
Source dataset
uspto-grants-2013_03
Patent number
US08394796B2

Reaction notes

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