3-Pyridinecarboxaldehyde → Ethyl 2-methyl-2-(pyridin-3-ylmethylamino)propanoate

HRID 2095078Notes

Reaction equation

[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[N:4][CH:3]=1.Cl.[NH2:10][C:11]1([C:14]([O:16][CH2:17][CH3:18])=[O:15])[CH2:13][CH2:12]1>>[CH3:12][C:11]([NH:10][CH2:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1)([CH3:13])[C:14]([O:16][CH2:17][CH3:18])=[O:15]

Participants

Reactant 2

HCID 103713-Pyridinecarboxaldehyde

HCID 386203Ethyl 1-aminocyclopropane-1-carboxylate hydrochloride

Product 1

HCID 59524391Ethyl 2-methyl-2-(pyridin-3-ylmethylamino)propanoateYield 95%

Procedure

Prepared as in Example 12-1b from nicotinaldehyde and ethyl 1-aminocyclopropanecarboxylate hydrochloride. Yield 95%, a white solid. MS 223 (MH+).

Sources & evidence

ORD record: ord-98882c2009a34a85932662ec79592a33
Source dataset: uspto-grants-2013_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08445692B2

Reaction notes

Loading…