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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362187Generated: November 3, 2026

1-Methyl-3-(methylaminomethyl)indole → HCID 66967302, compound

https://huagongshe.com/reaction/1362187

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-3-(methylaminomethyl)indoleHCID 10986778—
ReactantMethyl-(1-propyl-naphthalen-2-ylmethyl)amineHCID 59456959—
ReactantHCID 59456972HCID 59456972—
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—
ProductHCID 66967302HCID 6696730234%

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-(2,4-dioxo-1,2,3,4-tetrahydro-pyrido[2,3-d]pyrimidin-6-yl)acrylic acid 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 (0.16 g, 34%) was prepared as a tan solid and as a mixture of amide rotamers; 1H NMR (300 MHz, DMSO-d6) δ 11.84 (s, 1H), 11.53 (s, 1H), 8.91 (s, 1H), 8.73-8.66 (m, 1H), 7.78-7.30 (m, 5H), 7.17-7.12 (m, 1H), 7.03-6.98 (m, 1H), 4.96-4.73 (m, 2H), 3.76 (s, 3H), 3.07-2.90 (m, 3H); MS (ESI) m/e 390 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-d96ab4ba11b0495f8a7b44b52ebce160
Source noteuspto-grants-2011_02