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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180739Generated: October 30, 2026

HCID 58979652, compound → HCID 10174359, compound

https://huagongshe.com/reaction/1180739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58979652HCID 58979652—
ReactantHCID 58979693HCID 58979693—
ProductHCID 10174359HCID 10174359—

Reaction Steps

[1-(3-phenylpropyl)cyclobutyl]methyl(1S)-1-(oxo{[(1R)-1-phenylethyl]amino}acetyl)pentylcarbamate was prepared as in example 6c except that [1-(3-phenylpropyl)cyclobutyl]methyl(1S)-1-(1-hydroxy-2-oxo-2-{[(1R)-1-phenylethyl]amino}ethyl)pentylcarbamate was substituted for [1-(2-phenylethyl)cyclobutyl]methyl(1S)-1-(1-hydroxy-2-oxo-2-{[(1R)-1-phenylethyl]amino}ethyl)pentylcarbamate. M.P.=91-93° C. Elemental analysis: Theory; C=73.14%, H=8.18%, N=5.69%. Found; C=72.81%, H=8.22%, N=5.82%. 1H NMR (400 MHz, DMSO-d6) δ 9.10 (d, J=8 Hz, 1H), 7.45 (d, J=8 Hz, 1H), 7.11-7.26 (m, 10H), 4.91 (qnt, J=8 Hz, 1H), 4.70 (m, 1H), 3.85 (s, 2H), 2.50 (m, 2H), 1.55-1.74 (m, 6H), 1.13-1.45 (m, 13H), 0.74 (t, J=7 Hz, 13H). ES-LCMS m/z 515 (M+Na). HRMS C30H40N2O4 m/z 515.2886 (M+Na)Cal; 515.2891 (M+Na)Obs.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282512B2
Source datasetuspto-grants-2007_10
ORD IDord-87550c72fd354a1d852207929122d2f1
Source noteuspto-grants-2007_10