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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306738Generated: October 25, 2026

(2-Methanesulfonylethyl)(methyl)amine → HCID 22609841, compound

https://huagongshe.com/reaction/2306738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Methanesulfonylethyl)(methyl)amineHCID 3856040—
ReactantHCID 21952306HCID 21952306—
ProductHCID 22609841HCID 2260984139%

Reaction Steps

In an analogous manner to Example 10, 5-(4-(4-Benzyloxy-phenylamino)-quinazolin-6-yl)-furan-2-carbaldehyde hydrochloride (0.217 g, 0.474 mmol) was reacted with N-methyl-N-(2-methanesulphonyl-ethyl)amine (0.411 g, 3.0 mmol). Purification by silica gel chromatography, eluting with 2-3% MeOH/CHCl3, followed by trituration with ether, gave the title compound as a pale yellow solid (0.100 g, 0.184 mmol, 39%); δH [2H6]DMSO 9.84 (1H, s), 8.63 (1H, s), 8.48 (1H, s), 8.12 (1H, d), 7.78 (1H, d), 7.68 (2H, d), 7.13-7.52 (5H, m), 7.02-7.10 (3H, m), 6.55 (1H, d), 5.14 (2H, s), 3.70 (2H, s), 3.35-3.44 (2H, obscured by water), 3.05 (3H, s), 2.84 (2H, t), 2.28 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828320B2
Source datasetuspto-grants-2004_12
ORD IDord-c0ebf79d1c67434ca5c31c56111d353d
Source noteuspto-grants-2004_12