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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373850Generated: November 1, 2026

Methyl iodide → HCID 23023993, compound

https://huagongshe.com/reaction/1373850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropyl EtherHCID 7914—
ReactantSodium hydrideHCID 24758—
ReactantHCID 23023970HCID 23023970—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 23023993HCID 2302399391.4%

Reaction Steps

Under an argon atmosphere, to a suspension of sodium hydride (content 60%, 26.4 g, 0.661 mol) in N,N-dimethylformamide (530 ml, 2.5 v/w) were successively added dropwise a solution of methyl 4-((4-(4-nitrophenyl)-2-thiazolyl)aminomethyl)benzoate (212.4 g, 0.575 mol) obtained in Example 1(2) in N,N-dimethylformamide (743 ml, 3.5 v/w) and methyl iodide (41.2 ml, 0.661 mol) at 10° C. or below, and the mixture was stirred at room temperature for 2 hr. Sodium hydride (content 60%, 2.3 g, 0.057 mol) was added and the mixture was stirred at room temperature for 1 hr. The reaction mixture was added dropwise to water (2120 ml, 10.0 v/w) at 10° C. or below, and, after stirring at room temperature for 30 min., diisopropyl ether (848 ml, 4.0 v/w) was added and the mixture was stirred for 2 hr. The precipitated crystals were collected by filtration, washed successively with diisopropyl ether (424 ml) and water (424 ml) and dried in vacuo to give the title compound (201.9 g, yield 91.4%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163952B2
Source datasetuspto-grants-2007_01
ORD IDord-fac24893fa3a49f296f7528bf9b3e31a
Source noteuspto-grants-2007_01