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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441186Generated: November 1, 2026

HCID 131719355, compound → HCID 131719354, compound

https://huagongshe.com/reaction/1441186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131719355HCID 131719355—
ReactantHCID 131719356HCID 131719356—
CatalystPalladiumHCID 23938—
SolventN,N-dimethylformamide ethanolHCID 19794673—
ProductHCID 131719354HCID 131719354—

Reaction Steps

More specifically exemplified, the protected peptide, DAT-N-Me-Val-Ile-Asp(NEt2)-Asp(OBzl)-Leu-OH was assembled by the preceding procedure on a BHA photoresin using BOP/HOBt as the coupling agent, followed by cleavage of the resulting protected peptide resin by photolysis under argon at -5° for 6 h. DMF:EtOH (4:1) was used as the photolysis medium. Deprotection of the cleavage product was effected by hydrogenolysis using 5% Pd/C as catalyst. Purification of the product was done by HPLC, the product being dissolved in 0.1N aqueous NH4OH solution and the solution adjusted to pH6 with 0.1N aqueous AcOH. Whatman Partisil® 100DS-3 C-18 column (2.2×50 cm2), 10 micron particle size, was used. Elution was done with a gradient of acetonitrile and 0.06% aqueous TFA. Pure fractions (determined by analytical HPLC) were pooled and lyophilized to give DAT-N-Me-Val-Ile-Asp(NEt2)-Asp-Leu-OH. MS: 791 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05502036
Source datasetuspto-grants-1996_03
ORD IDord-23d4967d04354312b7972a4b4f963f14
Source noteuspto-grants-1996_03