Trifluoroacetic acid → (R)-ethyl 3-(pyrrolidin-2-ylmethoxy)picolinate

HRID 2406795Notes

Reaction equation

HRID 2406795 reaction equation
C(OC([N:8]1[CH2:12][CH2:11][CH2:10][C@@H:9]1[CH2:13][O:14][C:15]1[C:16]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[N:17][CH:18]=[CH:19][CH:20]=1)=O)(C)(C)C.FC(F)(F)C(O)=O>ClCCl>[NH:8]1[CH2:12][CH2:11][CH2:10][C@@H:9]1[CH2:13][O:14][C:15]1[C:16]([C:21]([O:23][CH2:24][CH3:25])=[O:22])=[N:17][CH:18]=[CH:19][CH:20]=1

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 86666097(R)-ethyl 3-((1-(tert-butoxycarbonyl)pyrrolidin-2-yl)methoxy)picolinate

Product 1

HCID 86666098(R)-ethyl 3-(pyrrolidin-2-ylmethoxy)picolinate

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of (R)-ethyl 3-((1-(tert-butoxycarbonyl)pyrrolidin-2-yl)methoxy)picolinate (1.00 g, 285 mmol, EXAMPLE 33 Step 1) in dichloromethane (10 mL) was added trifluoroacetic acid (3 mL) at room temperature. After being stirred at room temperature for 8 h, the volatile was evaporated to afford 1.36 g (quant.) of the title compound that was used directly in the next step without further purification.

Workup

  1. customthe volatile was evaporated

Sources & evidence

ORD record
ord-52d3ccf9da3644dbb7d534ece4712aca
Source dataset
uspto-grants-2014_08
Patent number
US08809380B2

Reaction notes

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