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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077968Generated: October 29, 2026

6-carboxy-N2-[[[carboxy-2-[(1-oxoheptyl)amino]ethyl]amino]carbonyl]-N6-[(1,1-dimethylethoxy)carbonyl]-L-lysyl-D-alanine → N-[6-carboxy-N2-[[[2-carboxy-2-[(1-oxoheptyl)amino]-ethyl]amino]carbonyl]-L-lysyl]-D-alanine

https://huagongshe.com/reaction/1077968

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-carboxy-N2-[[[carboxy-2-[(1-oxoheptyl)amino]ethyl]amino]carbonyl]-N6-[(1,1-dimethylethoxy)carbonyl]-L-lysyl-D-alanineHCID 86749718—
SolventTrifluoroacetic acidHCID 6422—
ProductN-[6-carboxy-N2-[[[2-carboxy-2-[(1-oxoheptyl)amino]-ethyl]amino]carbonyl]-L-lysyl]-D-alanineHCID 54072783—

Reaction Steps

To 85.9 mg of 1b-5 under argon is treated with 500 μl of TFA according to Example 80. The volatiles are evaporated to a residue which is triturated with ether 3x and the ether is decanted. The residue is dried to give 77.9 mg of 1b-11 as a white solid. NMR(CD3OD) δ 0.80(t,3H), 2.16(t,2H), 3.22(br s,5H), 3.58(m,2H), 3.85(m,1H), 4.15(m,1H), 4.30(d,1H), 4.40(m,1H); MS(HR--FAB) m/z 526.2482 (M+H, calcd for C21H38N5O9 526.2489).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05545662
Source datasetuspto-grants-1996_08
ORD IDord-b7fe7d6079704de59021c98c63096ae6
Source noteuspto-grants-1996_08