(R)-3-(pyrrolidin-2-ylmethoxy)picolinamide dihydrochloride → HCID 178513798, compound

HRID 869652Notes

Reaction equation

HRID 869652 reaction equation
Cl.Cl.[NH:3]1[CH2:7][CH2:6][CH2:5][C@@H:4]1[CH2:8][O:9][C:10]1[C:11]([C:16]([NH2:18])=[O:17])=[N:12][CH:13]=[CH:14][CH:15]=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:3]2[CH2:7][CH2:6][CH2:5][C@@H:4]2[CH2:8][O:9][C:10]2[C:11]([C:16]([NH2:18])=[O:17])=[N:12][CH:13]=[CH:14][CH:15]=2)=[O:28])[CH2:25][CH2:26]1

Participants

4

Reactant 3

HCID 66960633(R)-3-(pyrrolidin-2-ylmethoxy)picolinamide dihydrochlorideHCID 178493765HCID 178493765, compoundHCID 178525710HCID 178525710, compound

Product 1

HCID 178513798HCID 178513798, compound

Procedure

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

Sources & evidence

ORD record
ord-5a09cedd43d648ce95100ba7bb68a778
Source dataset
uspto-grants-2015_03
Patent number
US08969383B2

Reaction notes

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