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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711873Generated: November 2, 2026

N-methyl(3-methylbenzo[b]thiophen-2-yl)methanamine → HCID 66967401, compound

https://huagongshe.com/reaction/1711873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl(3-methylbenzo[b]thiophen-2-yl)methanamineHCID 22593745—
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 66966216HCID 66966216—
SolventMethanolHCID 887—
ProductHCID 66967401HCID 6696740162%

Reaction Steps

According to the procedure of Example 1, except substituting methyl-(3-methyl-benzo[b]thiophen-2-ylmethyl)amine for the methyl-(1-propyl-naphthalen-2-ylmethyl)amine, and substituting (S)-(E)-3-(10-oxo-2,3,4,9,10,10a-hexahydro-1H-3a,8,9-triaza-benzo[f]azulen-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 (0.15 g, 62%) was prepared as a tan powder: [α]25D+167.8° (c 1.05, methanol); 1H NMR (300 MHz, DMSO-d6) δ 12.33 (br s, 1H), 11.30 (br s, 1H), 8.84 (s, 1H), 8.33 (s, 1H), 7.89-7.86 (m, 1H), 7.75-7.72 (m, 1H), 7.65-7.55 (m, 1H), 7.42-7.31 (m, 3H), 5.13-4.90 (m, 2H), 4.47-4.22 (m, 2H), 3.61 (br s, 1H), 3.42-3.39 (br s, 4H), 3.17-2.95 (m, 3H), 2.42 (s, 3H), 2.10-1.88 (2H); MS (ESI) m/e 447 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790709B2
Source datasetuspto-grants-2010_09
ORD IDord-2d269dc5249c4916922cebfc51e34927
Source noteuspto-grants-2010_09