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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362190Generated: November 3, 2026

methyl((1-methyl-1H-indol-2-yl)methyl)amine → HCID 59456941, compound

https://huagongshe.com/reaction/1362190

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl((1-methyl-1H-indol-2-yl)methyl)amineHCID 11401058—
ReactantHCID 22139032HCID 22139032—
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—
ProductHCID 59456941HCID 5945694128%

Reaction Steps

According to the procedure of Example 1 (a), except substituting methyl-(1-methyl-1H-indol-2-ylmethyl)amine for the methyl-(1-propyl-naphthalen-2-ylmethyl)amine, and substituting (E)-3-[6-amino-5-(2-carboxy-ethyl)pyridin-3-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 (0.37 g, 28%) was prepared as an off-white powder and as a mixture of amide rotamers: 1H NMR (300 MHz, DMSO-d6) δ 8.07 (m, 1H), 7.75-7.68 (m, 1H), 7.49-7.34 (m, 5H), 7.11-6.98 (m, 5H), 6.39-6.12 (m, 4H), 4.95-4.68 (m, 4H), 3.69 (s, 3H), 3.61 (s, 3H), 3.02-2.71 (m, 10H); MS (ESI) m/e 549 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-4803bf231290469fb00c8aefba78efab
Source noteuspto-grants-2011_02