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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442635Generated: November 3, 2026

Dicyclohexylcarbodiimide → HCID 131727877, compound

https://huagongshe.com/reaction/1442635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantFmoc-D-leucineHCID 1549477—
ReactantHCID 131727878HCID 131727878—
SolventDimethylformamideHCID 6228—
SolventPiperidineHCID 8082—
ProductHCID 131727877HCID 13172787717.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

Dipeptide Fmoc-NH-L-Ile-S-Phe-CH2OH (1b) (2.0 g, 4.11 mmol) was taken in 20% piperidine in DMF (20 mL) and stirred for 15 minutes at 25° C., TLC examination showed complete removal of the Fmoc protecting group (NH2-L-Ile-S-Phe-CH2OH), further confirmed by LC/MS examination, which showed M+−1 (263.3) peak. The reaction mixture was concentrated in vacuo, excess of the piperidine was removed by co-evaporating with toluene (2×20 mL), the free amino dipeptide was further dried over high vacumn for 30 minutes, and then redissolved in dry DMF (5 mL) and added to the mixture of N-(9-fluorenylmethoxycarbonyl)-D-leucine (1.59 g, 4.52 mmol), DCC (931 mg, 4.52 mmol) and HOBt (610.0 mg, 4.52 mmol) in dry DMF (150 mL) at 25° C. The stirring was further continued for 14 h at 25° C. After 14 h white colored crystals precipitated out (DCU), which was filtered. The filterate was checked on TLC (5% MeOH: CH2Cl2) which showed formation of a new compound at higher Rf (0.5), LC/MS also showed molecular ion peak corresponding to the tripeptide 2b with other impurities peaks. The crude product was chromatographed on silica gel (Silica gel 60, 63-200μ) column and eluted with 4% MeOH: CH2Cl2 to give 450 mg of the tripeptide Fmoc-NH-D-Leu-L-Ile-S-Phe-CH2OH (2b) as a white solid. Checked on LC/MS which showed M++1 (600.3) and M++Na (622.3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659244B2
Source datasetuspto-grants-2010_02
ORD IDord-29746daa39d042048dae7a07838cc7be
Source noteuspto-grants-2010_02