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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156951Generated: November 2, 2026

Dicyclohexylcarbodiimide → BOC-(D)-Asn-Gly-MePhe-NHNHCSNH2

https://huagongshe.com/reaction/1156951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant3a,4,7,7a-Tetrahydro-2-hydroxy-4,7-methano-1H-isoindole-1,3(2H)-dioneHCID 89529—
ReactantBoc-D-asparagineHCID 1623168—
ReactantHCID 12802635HCID 12802635—
SolventDimethylformamideHCID 6228—
SolventTrifluoroacetic acidHCID 6422—
ProductBOC-(D)-Asn-Gly-MePhe-NHNHCSNH2HCID 12802643—

Reaction Steps

In 10 ml of trifluoroacetic acid is dissolved 0.80 g of BOC-Gly-MePhe-NHNHCSNH2 and the solution is shaken for 10 minutes, concentrated, treated with ether and filtered to obtain a powder. This powder is dissolved in 10 ml of DMF, and after ice-cooling, the solution is neutralized with 0.20 ml of TEA followed by addition of 0.47 g of BOC-(D)-Asn-OH, 0.40 g of HONB and 0.45 g of DCC. The mixture is stirred for 20 hours, the precipitated DCU filtered off, the solvent distilled off and the residue dissolved in n-butanol. The solution is washed with a saturated aqueous solution of sodium hydrogen carbonate and water in that order and dried over anhydrous sodium sulfate. The solvent is distilled off and the residue is treated with ether and filtered to obtain a powder, which is further reprecipitated from methanol-ether. Yield 0.69 g; m.p. 124°-127° C.; [α]D24 -42.5° (c=1.0, DMF); Rf1 0.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04337247
Source datasetuspto-grants-1982_06
ORD IDord-f4fbd834bdee40638a0179a2ed702840
Source noteuspto-grants-1982_06