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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523354Generated: October 26, 2026

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

https://huagongshe.com/reaction/523354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantCyclopentyl methyl etherHCID 138539—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-(9-Fluorenylmethoxycarbonyl)-O-tert-butylthreonineHCID 6364643—
ReactantH-Ser(tBu)-OBzlHCID 53722581—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductFmoc-Thr(tBu)-Ser(tBu)-OBzlHCID 131735566—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334302B2
Source datasetuspto-grants-2016_05
ORD IDord-47ff74d2bf5b49b4b9f30fe9177fb66e
Source noteuspto-grants-2016_05