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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362363Generated: October 29, 2026

N-Methyl-N-[(2-methyl-1H-indol-3-yl)methyl]amine → HCID 59277609, compound

https://huagongshe.com/reaction/1362363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Methyl-N-[(2-methyl-1H-indol-3-yl)methyl]amineHCID 10954023—
Reactant3-(4-Methyl-2-oxo-2,3,4,5-tetrahydro-1H-pyrido[2,3-e][1,4]diazepin-7-yl)-acrylic acidHCID 66966201—
ProductHCID 59277609HCID 592776099.9%

Reaction Steps

According to the method of example 35g, methyl-(2-methyl-1H-indol-3-ylmethyl)amine (115 mg, 0.66 mmol) and 3-(4-Methyl-2-oxo-2,3,4,5-tetrahydro-1H-pyrido[2,3-e][1,4]diazepin-7-yl)-acrylic acid (192 mg, 0.6 mmol) were coupled to give crude product. Purification by column chromatography (silica gel, CH2Cl2/MeOH/NH3, 9:4.55:0.05) gave title compound (24 mg, 9%) as a white solid and as a mixture of amide rotomers. 1H NMR (300 MHz, DMSO-d6) δ 8.48 (s, 1H), 7.95-8.01 (m, 2H), 7.56-7.60 (m, 2H), 7.47-7.50 (m, 1H), 7.16-7.26 (m, 2H), 6.92-7.05 (m, 2H), 3.90 (s, 2H), 3.56 (s, 2H), 3.02 (s, 2H), 2.93 (s, 3H), 2.83 (s, 3H), 2.46 (s, 3H); MS (ESI) m/e 404 (C23H25N5O2+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-202f0af8204b4f98a1ad4026b6d57df6
Source noteuspto-grants-2011_02