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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65374Generated: October 29, 2026

Dicyclohexylcarbodiimide → HCID 178455946, compound

https://huagongshe.com/reaction/65374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantN-[(Phenylmethoxy)carbonyl]-L-leucyl-L-valineHCID 14488993—
ReactantHCID 178455957HCID 178455957—
ReactantHCID 178455961HCID 178455961—
SolventDimethylformamideHCID 6228—
ProductHCID 178455946HCID 178455946—

Reaction Steps

Z-Leu-Val-Ile-His-Lys(BOC)-OMe: 300 mg of Z-Leu-Val-OH, 454 mg of H-Ile-His-Lys(BOC)-OMe (manufactured as discribed in European Patent Applicaiton No. 111 266) and 136 mg of HOBt are dissolved in 5 ml of DMF, cooled to 0° and 198 mg of DCCI are added. After stirring briefly, the whole is left to stand overnight at 0° and for a further 24 hours at room temperature and then the DCH which has crystallised out is filtered off. The filtrate is concentrated in a high vacuum at 40° and the oily residue is dissolved in 12 ml of methanol/glacial acetic acid/H20 (94:3:3) and heated for 1 hour at 60°. The solution is again concentrated to dryness and the residue is purified by Craig distribution in the system methanol/acetate buffer/ethylene chloride/chloroform 10:3:8:4 (acetate buffer: 14.3 ml of glacial acetic acid and 9.6 g of ammonium acetate in 1000 ml of water) over 800 stages. The fractions pure according to thin layer chromatography (K=0.26) are combined, concentrated to dryness, pulverised and subsequently dried in a high vacuum at 40°. Rf (B17)=0.70, Rf (S4)=0.75.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04613676
Source datasetuspto-grants-1986_09
ORD IDord-1dc1bbfc55d2412b95ccb52dc3e5dd47
Source noteuspto-grants-1986_09