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HRID 1796213作成日:2026年10月27日

Pyridine → (R)-2-(4-Bromo-2-fluoro-phenylcarbamoyl)-pyrrolidine-1-carboxylic acid 9H-fluoren-9-ylmethyl ester

https://huagongshe.com/reaction/1796213

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Thionyl ChlorideHCID 24386—
反応物4-Bromo-2-fluoroanilineHCID 123050—
反応物(2R)-1-((9H-fluoren-9-ylmethoxy)carbonyl)pyrrolidine-2-carboxylic acidHCID 688136—
溶媒DichloromethaneHCID 6344—
生成物(R)-2-(4-Bromo-2-fluoro-phenylcarbamoyl)-pyrrolidine-1-carboxylic acid 9H-fluoren-9-ylmethyl esterHCID 68807238—

反応手順

Fmoc-D-Pro (1.2 g, 3.56 mmol) was suspended in 10 mL dry dichloromethane (DCM), cooled in an ice water bath, and then thionyl chloride (0.78 mL, 10.7 mmol) was added slowly. After addition was complete, the ice water bath was removed and the reaction was stirred at ambient temperature overnight. The solution was concentrated to dryness. The oil was redissolved in 20 mL dry DCM under an Ar atmosphere, and 4-bromo-2-fluoroaniline (0.81 g, 4.3 mmol) was added, followed by dry pyridine (0.87 mL, 10.7 mmol). The mixture was stirred at ambient temperature for 4 hours, then concentrated. The residue was redissolved in 100 mL EtOAc, washed with 1M HCl (3×50 mL), brine (2×50 mL), dried with MgSO4, filtered and concentrated to yield the title product as a sticky oil. (1.8 g, 99%) APCI (AP+): 509.2, 511.2 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07030141B2
出典データセットuspto-grants-2006_04
ORD IDord-27ec977d87b443c3923f8670a7c1734f
出典メモuspto-grants-2006_04