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HRID 2415492作成日:2026年10月25日

Triphenylphosphine → [2,2-Dimethyl-3-(2-methyl-4-pyrrolidin-1-yl-quinolin-7-yloxy)-propyl]-dimethyl-amine

https://huagongshe.com/reaction/2415492

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物3-(Dimethylamino)-2,2-dimethyl-1-propanolHCID 87919—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物2-Methyl-4-pyrrolidin-1-yl-quinolin-7-olHCID 135804118—
溶媒TetrahydrofuranHCID 8028—
溶媒Dichloromethane methanol ammonium hydroxideHCID 21896990—
生成物[2,2-Dimethyl-3-(2-methyl-4-pyrrolidin-1-yl-quinolin-7-yloxy)-propyl]-dimethyl-amineHCID 2264143923%

反応手順

A suspension of 114 mg (0.5 mmol) of 2-methyl-4-pyrrolidin-1-yl-quinolin-7-ol, product of example 2, 71 mg (0.53 mmol) of 3-dimethylamino-2,2-dimethyl-1-propanol, 196.7 mg (0.75 mmol) of triphenyl phosphine in THF (4 ml) was treated at RT with 123 μl (0.75 mmol) of diethyl azodicarboxylate and stirred at RT for 48 h. The precipitate that had formed was removed by filtration, the filtrate was concentrated in vacuo and the oily residue obtained was applied to silica gel column with CH2Cl2/MeOH/NH4OH (90:10:1) as eluent. The purified fractions were combined and concentrated in vacuo. The residue was taken up in ether, the crystalline solid that formed was filtered off by suction and dried in a high vacuum to give 24 mg (23%) of the desired [2,2-dimethyl-3-(2-methyl-4-pyrrolidin-1-yl-quinolin-7-yloxy)-propyl]-dimethyl-amine as an off-white solid. ISP mass spectrum, m/e: 342.4 (M+1 calculated for C21H31N3O: 342). (Further material, 30 mg, 29%, was obtained on concentration of the mother liquid and collection of the product as hydrochloride salt).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06818767B2
出典データセットuspto-grants-2004_11
ORD IDord-259de672192b44f9844b8fba7d869c1d
出典メモuspto-grants-2004_11