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HRID 2180118作成日:2026年10月27日

Triphenylphosphine → 4-Chloro-6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)cinnoline

https://huagongshe.com/reaction/2180118

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物1-PyrrolidinepropanolHCID 209342—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物4-Chloro-7-hydroxy-6-methoxycinnolineHCID 135752523—
溶媒DichloromethaneHCID 6344—
生成物4-Chloro-6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)cinnolineHCID 1127869018%

反応手順

To a solution of 4-chloro-7-hydroxy-6-methoxycinnoline (300 mg, 1.42 mmol), triphenylphosphine (747 mg, 2.85 mmol) and 3-(pyrrolidin-1-yl)propan-1-ol (276 mg, 2.1 mmol) in methylene chloride (12 ml) was added diethyl azodicarboxylate (449 μl, 2.85 mmol) dropwise and the mixture was stirred for 2 hours at ambient temperature. The volatiles were removed under vacuum and the residue was purified by column chromatography eluting with methylene chloride/methanol (90/10) followed by methylene chloride/methanol/methanol saturated with ammonia (89/10/1 followed by 85/10/5). The fractions containing the expected product were combined and evaporated to give 4-chloro-6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)cinnoline (80 mg, 18%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06887874B2
出典データセットuspto-grants-2005_05
ORD IDord-69bbf242a4eb4472863103edf67ac4cc
出典メモuspto-grants-2005_05