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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508051Generated: November 1, 2026

(2-(Methylthio)ethyl)amine → HCID 178503810, compound

https://huagongshe.com/reaction/1508051

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-(Methylthio)ethyl)amineHCID 87697—
ReactantHCID 178424524HCID 178424524—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 178503810HCID 17850381050.3%

Reaction Steps

The title compound was prepared by the procedure of Example 14, step (e) using 4-cyano-1H-imidazole-2-carboxylic acid [2-(4,4-dimethyl-cyclohex-1-enyl)-4-(1-hydroxy-1-methyl-ethyl)-phenyl]-amide (as prepared in Example 14, step (d), 120 mg, 0.317 mmol) and 2-methylsulfanyl-ethylamine (69.0 μL, 0.951 mmol). Silica gel chromatography (1-4% MeOH/DCM) afforded the title compound (72 mg, 50%) as a white solid. 1H-NMR (CD3OD; 400 MHz): δ 8.26 (d, 1H, J=8.6 Hz), 7.94 (s, 1H), 7.39 (dd, 1H, J=8.6, 2.3 Hz), 7.32 (d, 1H, J=2.3 Hz), 5.75 (m, 1H), 2.51-2.61 (m, 4H), 2.29-2.36 (m, 2H), 2.05-2.12 (m, 2H), 1.91 (s, 3H), 1.60 (t, 2H, J=6.3 Hz), 1.54 (s, 6H), 1.09 (s, 6H). Mass spectrum (ESI-neg, m/z): Calcd. for C25H33N5OS, 450.4 (M−H). found 450.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221797B2
Source datasetuspto-grants-2015_12
ORD IDord-2dd725e23af94824ae3fbd867ad00bd1
Source noteuspto-grants-2015_12