Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711880Generated: November 2, 2026

1-Methyl-3-(methylaminomethyl)indole → HCID 66967394, compound

https://huagongshe.com/reaction/1711880

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-3-(methylaminomethyl)indoleHCID 10986778—
ReactantMethyl-(1-propyl-naphthalen-2-ylmethyl)amineHCID 59456959—
Reactant(E)-3-(4-methyl-2-oxo-2,3,4,5-tetrahydro-1H-pyrido[2,3-e][1,4]diazepin-7-yl)acrylic acid hydrochlorideHCID 66966197—
ReactantHCID 66967035HCID 66967035—
ProductHCID 66967394HCID 6696739423%

Reaction Steps

According to the procedure of Example 1 (a), except substituting methyl-(1-methyl-1H-indol-3-ylmethyl)amine for the methyl-(1-propyl-naphthalen-2-ylmethyl)amine, and substituting (E)-3-(2-oxo-2,3-dihydro-oxazolo[4,5-b]pyridine-6-yl)acrylic acid hydrochloride for the (E)-3-(4-methyl-2-oxo-2,3,4,5-tetrahydro-1H-pyrido[2,3-e][1,4]diazepin-7-yl)acrylic acid hydrochloride, the title compound (0.075 g, 23%) was prepared as a light brown solid: 1H NMR (300 MHz, CDCl3) δ 8.28-8.24 (m, 1H), 7.82 (d, J=15.4 Hz, 1H), 7.71-7.49 (m, 2H), 7.37-6.87 (m, 5H), 4.88-4.86 (m, 2H), 3.78 (s, 3H), 3.16-3.12 (m, 3H); MS (ESI) m/e 363 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790709B2
Source datasetuspto-grants-2010_09
ORD IDord-21595f6c9aa94a8b95434123f396c155
Source noteuspto-grants-2010_09