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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 523355Erstellt: 23. Oktober 2026

(+-)-Mercaptosuccinic acid → H-Tyr(tBu)-Leu-OBzl

https://huagongshe.com/de/reaction/523355

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(+-)-Mercaptosuccinic acidHCID 6268—
EduktMethanesulfonic AcidHCID 6395—
EduktTriethylamineHCID 8471—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
EduktL-Leucine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1)HCID 6451312—
EduktFmoc-L-Tyr(tBu)-OHHCID 10895791—
LösungsmittelChloroformHCID 6212—
LösungsmittelSodium chloride; waterHCID 57417360—
ProduktH-Tyr(tBu)-Leu-OBzlHCID 131735567—

Reaktionsschritte

H-Leu-OBzl-TsOH salt (394 mg, 1.00 mmol) was dissolved in chloroform (10 ml), triethylamine (0.14 mL, 1.00 mmol), HOBt (14 mg, 0.10 mmol) and Fmoc-Tyr(tBu)-OH (506 mg, 1.10 mmol) were added, EDC.HCl (232 mg, 1.21 mmol) was added under ice-cooling, and the mixture was stirred at room temperature overnight. After completion of the reaction, to this solution were added under ice-cooling thiomalic acid (450 mg, 3.00 mmol) and DBU (1.49 mL, 10.00 mmol), and the mixture was stirred at room temperature for 3 hr. After completion of the reaction, to this solution was added dropwise under ice-cooling a mixture of MsOH (0.23 mL, 3.60 mmol) and chloroform (2.3 mL), chloroform (10 ml) and 20% brine (20 ml) were added to give an organic layer and an aqueous layer. Then, the aforementioned pH=9.0 washing was performed three times. The obtained organic layer was washed three times with 10% aqueous sodium carbonate solution (20 ml) and three times with 20% brine (20 ml) with stirring at room temperature, and the organic layer and the aqueous layer were partitioned. The obtained organic layer was dried over sodium sulfate and filtered to give a chloroform solution (20 ml) of H-Tyr(tBu)-Leu-OBzl. This chloroform solution was directly used in the next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09334302B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-67be36247e6542e0af2ffe054949a5a5
Quellennotizuspto-grants-2016_05