1-Aminopiperidine → HCID 71087732, compound

HRID 927412Notes

Reaction equation

HRID 927412 reaction equation
[O:1]1[CH2:6][CH2:5][CH:4]([C:7]2[N:12]=[C:11]([C:13]([OH:15])=O)[CH:10]=[CH:9][CH:8]=2)[CH2:3][CH2:2]1.[N:16]1([NH2:22])[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1>>[N:16]1([NH:22][C:13]([C:11]2[CH:10]=[CH:9][CH:8]=[C:7]([CH:4]3[CH2:3][CH2:2][O:1][CH2:6][CH2:5]3)[N:12]=2)=[O:15])[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1

Participants

3

Reactant 2

HCID 166581-AminopiperidineHCID 71087520HCID 71087520, compound

Product 1

HCID 71087732HCID 71087732, compound

Procedure

The title compound was synthesized in analogy to Example 1, using 6-(tetrahydro-pyran-4-yl)-pyridine-2-carboxylic acid and 1-piperidinamine (CAN 2213-43-6) as starting materials, MS (LC/MS): 290.2 [M+H]+.

Sources & evidence

ORD record
ord-97b33cf668644fedad369f99965b2834
Source dataset
uspto-grants-2016_03
Patent number
US09290451B2

Reaction notes

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