(2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acid → (E)-3-(6-aminopyridin-3-yl)-N-(7-fluoro-1H-indol-3-ylmethyl)-N-methylacrylamide

Participants

Role	Name	HCID	Charge
Reactant	(2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acid	HCID 10487224	—
Reactant	2,3-dihydro-8-(methylaminomethyl)-1H-3a-azacyclopenta[a]indene	HCID 22139048	—
Reactant	7-fluoro-3-(methylaminomethyl)-1H-indole	HCID 22139059	—
Reactant	(E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylic Acid Hydrochloride	HCID 66905305	—
Product	(E)-3-(6-aminopyridin-3-yl)-N-(7-fluoro-1H-indol-3-ylmethyl)-N-methylacrylamide	HCID 10041922	18%

Reaction Steps

According to the procedure of Example 24, except substituting 7-fluoro-3-(methylaminomethyl)-1H-indole (0.31 g, 1.74 mmole) for the 2,3-dihydro-8-(methylaminomethyl)-1H-3a-azacyclopenta[a]indene, and substituting (E)-3-(6-amino-pyridin-3-yl)acrylic acid (0.285 g, 1.74 mmole) for the (E)-3-(7-oxo-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)acrylic acid hydrochloride salt, the title compound (0.1 g, 18%) was prepared as a white powder: MS (ES) m/e 325 (M+H)+.

Provenance & Evidence

DOI	10.6084/m9.figshare.5104873.v1
Patent number	US07250424B2
Source dataset	uspto-grants-2007_07
ORD ID	ord-7d9f16f41a674a3e8a9928dd45846783
Source note	uspto-grants-2007_07