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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 523354생성일: 2026년 10월 26일

Sodium Carbonate → Fmoc-Thr(tBu)-Ser(tBu)-OBzl

https://huagongshe.com/reaction/523354

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Cyclopentyl methyl etherHCID 138539—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물N-(9-Fluorenylmethoxycarbonyl)-O-tert-butylthreonineHCID 6364643—
반응물H-Ser(tBu)-OBzlHCID 53722581—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물Fmoc-Thr(tBu)-Ser(tBu)-OBzlHCID 131735566—

반응 단계

To the CPME solution (35 mL) of H-Ser(tBu)-OBzl (2-OBzl(3,4,5-OPhy)-4-OMe) was added HOBt (71 mg, 0.43 mmol), Fmoc-Thr(tBu)-OH (1.00 g, 2.51 mmol), EDC.HCl (529 mg, 2.76 mmol) and DMF (10 ml) were added under ice-cooling, and the mixture was stirred at room temperature overnight. After completion of the reaction, to the reaction solution was added 20% brine (30 ml) to give an organic layer and an aqueous layer. While stirring the obtained organic layer and aqueous layer, 10% aqueous sodium carbonate solution was added dropwise until the pH of the aqueous layer became 6.0, and the organic layer and the aqueous layer were partitioned (hereinafter this operation is sometimes to be abbreviated as “pH=6.0 washing”). The pH-6.0 washing was further repeated twice. The solvent in the obtained organic layer was evaporated under reduced pressure, the residue was dissolved in cyclohexane (40 ml), and the mixture was washed four times with 80% by volume of aqueous acetonitrile solution (30 ml) with stirring, and the organic layer and the aqueous layer were partitioned. The obtained organic layer was dried over sodium sulfate and filtered. The solvent in the obtained filtrate was evaporated under reduced pressure to give Fmoc-Thr(tBu)-Ser(tBu)-OBzl (2-OBzl(3,4,5-OPhy)-4-OMe).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09334302B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-47ff74d2bf5b49b4b9f30fe9177fb66e
출처 메모uspto-grants-2016_05