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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006265Generated: October 31, 2026

Methylamine → HCID 22676742, compound

https://huagongshe.com/reaction/1006265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantHCID 22676782HCID 22676782—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22676742HCID 22676742—

Reaction Conditions

Temperature120 °C

Reaction Steps

A reaction mixture of ethyl 5-(2-chloroethoxy)-1-(3-methoxybenzyl)-3-(4-methoxyphenyl)-1H-indole-2-carboxylate (Example 152, 290 mg, 0.588 mmol) and methylamine in tetrahydrofuran (2 M, 40 ml) was sealed in a stainless steel vessel (100 ml, bomb) at 0° C. Then it was heated and stirred at 120° C. for 3 days in a oil bath. Oil bath was removed and the bomb was allowed to cooled to room temperature before opened. The reaction solution was transferred to an round-bottomed flask and solvent was concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with 1N NaOH. The organic phase was dried over anhydrous sodium sulfate, concentrated and purified by flash column (silica gel, hexane: ethyl acetate=1:1 to ethyl acetate:2M NH3/ methanol =9:1). 214 mg desired product was obtained as a light yellow oil in 75%. MS (M+H)=489.2, Rf=0.28 (ethyl acetate:2M NH3/methanol=4:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787651B2
Source datasetuspto-grants-2004_09
ORD IDord-bb7a1bab0b9d4a44a543c6e2360b2df9
Source noteuspto-grants-2004_09