2-Pyridineethanamine → HCID 21103273, compound

HRID 1354079Notes

Reaction equation

C([O:3][C:4]([CH2:6][N:7]([S:15]([C:18]1[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=1)(=[O:17])=[O:16])[CH:8]([CH2:13]O)[C:9]([O:11][CH3:12])=[O:10])=O)C.[NH2:26][CH2:27][CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][N:30]=1>>[CH3:25][O:24][C:21]1[CH:20]=[CH:19][C:18]([S:15]([N:7]2[CH2:6][C:4](=[O:3])[N:26]([CH2:27][CH2:28][C:29]3[CH:34]=[CH:33][CH:32]=[CH:31][N:30]=3)[CH2:13][CH:8]2[C:9]([O:11][CH3:12])=[O:10])(=[O:16])=[O:17])=[CH:23][CH:22]=1

Participants

Reactant 2

HCID 759192-Pyridineethanamine

HCID 11234214HCID 11234214, compound

Product 1

HCID 21103273HCID 21103273, compound

Procedure

A title compound was prepared by the same method as in Example 4, except that the compound of Example 3 and 2-(2-aminoethyl)pyridine were used to prepare an oil (yield 74%).

Sources & evidence

ORD record: ord-ed36e07385354546a365839df99a6b1b
Source dataset: uspto-grants-2007_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07223751B2

Reaction notes

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