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HRID 433034作成日:2026年10月25日

Triphenylphosphine → HCID 178512850、化合物

https://huagongshe.com/reaction/433034

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物DiisopropylcarbodiimideHCID 12734—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物4-Bromo-3,5-dihydroxybenzoic acidHCID 86023—
反応物2,4-Dichlorophenethyl alcoholHCID 2734099—
反応物Diisopropyl azodicarboxylateHCID 5363146—
反応物HCID 178454311HCID 178454311—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178512850HCID 178512850—

反応手順

Rink resin (500 mg; loading 0.3 mmol/g) functionalized with Arg(Boc)2 was coupled with 176 mg of 3,5-dihydroxy-4-bromobenzoic acid in the presence of DIC (110 mg) and HOBt (78 mg) in DMF. The resin was then washed and treated with a 30% solution of benzyltrimethylammonium hydroxide in DMF for 1 h. The resin was washed with DMF, 10% acetic acid in DMF, DMF, and DCM and dried in vacuo for 3 h. The dried resin was washed with anhydrous THF and mixed with 0.2 mmol of triphenylphosphane and 0.2 mmol of 2-(2,4-dichlorophenyl)ethanol in 2 ml of dry THF. The suspension of the resin was cooled in a refrigerator for 16 min and 50 μl (0.2 mmol) of DIAD in 0.5 ml of dry THF were added. Coupling was continued overnight at room temperature. The resin was washed with dry THF and the coupling was repeated for additional 8 h. The resin was washed and dried, and the final product was cleaved off and processed as described in Example 1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06664393B2
出典データセットuspto-grants-2003_12
ORD IDord-6b819f116e134274b935d0f22d796e7d
出典メモuspto-grants-2003_12