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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 433036생성일: 2026년 10월 25일

Triphenylphosphine → (s)-2-Amino-n-(1-carbamoyl-4-guanidino-butyl)-5-[2-(2,4-dichlorophenyl)ethoxy]benzamide

https://huagongshe.com/reaction/433036

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물5-Hydroxy-2-nitrobenzoic acidHCID 11882—
반응물DiisopropylcarbodiimideHCID 12734—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물2,4-Dichlorophenethyl alcoholHCID 2734099—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물HCID 178454311HCID 178454311—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물(s)-2-Amino-n-(1-carbamoyl-4-guanidino-butyl)-5-[2-(2,4-dichlorophenyl)ethoxy]benzamideHCID 178512851—

반응 단계

Rink resin (306 mg; loading 0.43 mmol/g) functionalized with Arg(Boc)2 was coupled with 146 mg of 5-hydroxy-2-nitrobenzoic acid in the presence of DIC (136 mg) and HOBt (140 mg) in DMF (2 ml) for 3 h at room temperature. The resin was then washed and treated with a 15% solution of benzyltrimethylammonium hydroxide in DMF for 60 min. The resin was washed with DMF, 10% acetic acid in DMF, DMF and DCM and dried in vacuo for 4 h. The dried resin was washed with anhydrous THF and mixed with 534 mg (2 mmol) of triphenylphosphane, 422 mg (2 mmol) of 2-(2,4-dichlorophenyl)ethanol and 400 μl (2 mmol) of DIAD in dry THF. The mixture was kept overnight at room temperature. The resin was washed and treated with 415 mg of tin dichloride monohydrate in 2 ml of DMF and 0.5 ml of trifluoroethanol. The reduction was continued overnight at room temperature. The resin was washed and dried, and the final product was cleaved off and processed as described in Example 1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06664393B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-5f2d0b808a76495195fdc7ec8cb0a7f9
출처 메모uspto-grants-2003_12