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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066711Generated: November 1, 2026

Acetic Anhydride → HCID 131722627, compound

https://huagongshe.com/reaction/1066711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 10070574HCID 10070574—
ReactantHCID 131722628HCID 131722628—
SolventDimethylformamideHCID 6228—
ProductHCID 131722627HCID 131722627—

Reaction Steps

The title compound was obtained by analogous manner as described in Example 18, but using BocTyr(PO3Et2)OH. The N-acetylation was performed by treatment of crude H—Tyr(PO3Et2)—Val—Asn—Val—NH2 with 1.5 equiv. of DIEA and 5 equiv. of acetic anhydride in DMF for 2 h at 25° C. The final compound was obtained with chromatographic purity (HPLC) of 90.0%. Amino acid ratios: Val 2 (2); Asx 1.17 (1); Tyr 0.87 (1). Peptide content: 83%. FAB mass spectroscopy; m/z 671 [M—H]+. (MW 670.1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245742B1
Source datasetuspto-grants-2001_06
ORD IDord-5353513a0c4f42509da40dcf791777d5
Source noteuspto-grants-2001_06