(R)-ethyl 3-(pyrrolidin-2-ylmethoxy)picolinate → HCID 178470240, compound

HRID 2406796Notes

Reaction equation

HRID 2406796 reaction equation
[NH:1]1[CH2:5][CH2:4][CH2:3][C@@H:2]1[CH2:6][O:7][C:8]1[C:9]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[N:10][CH:11]=[CH:12][CH:13]=1.[F:19][C:20]([F:31])([F:30])[C@H:21]1[CH2:26][CH2:25][C@H:24]([C:27](O)=[O:28])[CH2:23][CH2:22]1.COC1C=C(OC[C@H]2CCCN2C([C@H]2CC[C@H](C(F)(F)F)CC2)=O)C(C(O)=O)=NC=1>>[F:19][C:20]([F:30])([F:31])[C@H:21]1[CH2:22][CH2:23][C@H:24]([C:27]([N:1]2[CH2:5][CH2:4][CH2:3][C@@H:2]2[CH2:6][O:7][C:8]2[C:9]([C:14]([O:16][CH2:17][CH3:18])=[O:15])=[N:10][CH:11]=[CH:12][CH:13]=2)=[O:28])[CH2:25][CH2:26]1

Participants

4

Reactant 3

HCID 86666098(R)-ethyl 3-(pyrrolidin-2-ylmethoxy)picolinateHCID 178493765HCID 178493765, compoundHCID 178525710HCID 178525710, compound

Product 1

HCID 178470240HCID 178470240, compound

Procedure

The title compound was prepared according to the procedure described in Step 5 of EXAMPLE 31 using (R)-ethyl 3-(pyrrolidin-2-ylmethoxy)picolinate bis(trifluoroactetic acid) salt (EXAMPLE 34 Step 1) and trans-4-(trifluoromethyl)cyclohexanecarboxylic acid instead of ammonium chloride and 5-methoxy-3-(((R)-1-(trans-4-(trifluoromethyl)cyclohexanecarbonyl)pyrrolidin-2-yl)m ethoxy)picolinic acid.

Sources & evidence

ORD record
ord-514fdfaa2f8f4065b4f983f115ea669c
Source dataset
uspto-grants-2014_08
Patent number
US08809380B2

Reaction notes

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