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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469464Generated: October 31, 2026

Methylamine → HCID 68283926, compound

https://huagongshe.com/reaction/1469464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantHCID 86677141HCID 86677141—
ProductHCID 68283926HCID 68283926—

Reaction Steps

A solution of 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)-1-(pyridin-4-yl)ethyl methanesulfonate (250 mg, 0.62 mmol) in methyl amine (3 mL, 40% in water) was stirred at 90° C. for 12 h. The progress of reaction was monitored by LCMS. The reaction mixture was extracted with EtOAc. The organic layer was dried and concentrated to get the crude product, which was purified by reverse phase HPLC to obtain the 2-(1,2,3,4-tetrahydro-2,8-dimethylpyrido[4,3-b]indol-5-yl)-N-methyl-1-(pyridin-4-yl)ethanamine. 1H NMR (CDCl3, freebase): δ (ppm): 8.59 d (2H), 7.3 d (2H), 7.29 d (1H), 7.23 s (1H), 7.03 d (1H), 4.19 m (1H), 4.03 m (2H), 3.66 dd (2H), 2.8 m (3H), 2.6 m (1H), 2.55 s (3H), 2.47 s (3H), 2.18 s (3H). Chiral HPLC provided enantiomers 151a and 151b.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006263B2
Source datasetuspto-grants-2015_04
ORD IDord-e83dde3e1af542748eae01455508f489
Source noteuspto-grants-2015_04