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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061319Generated: November 3, 2026

HCID 10626009, compound → HCID 10627031, compound

https://huagongshe.com/reaction/1061319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10626009HCID 10626009—
Reactant(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamideHCID 12047933—
ProductHCID 10627031HCID 10627031—

Reaction Steps

The title compound was prepared from (2S)-2-[4-(4-oxo-piperidine-1-yl)-benzoylamino]-pentanedioic acid dibenzyl ester (which was obtained in Example 156) and N-[ 5-((1R)-2-amino-1-hydroxy-ethyl)-2-hydroxy-phenyl]-methanesulfonamide (which was obtained in Example 10) according to the procedure of Example 179 as a white solid; mp >230° C. (decomposed); 1H NMR (300 MHz, DMSO-d6) δ 1.40-1.60 (m, 2H), 1.90-2.10 (m, 4H), 2.31 (t, J=7.5 Hz, 2H), 2.65-3.20 (m, 7H), 3.00 (s, 3H), 3.85-4.00 (m, 2H), 4.25-4.35 (m, 1H), 4.65-4.80 (m, 1H), 6.88 (d, J=8.4 Hz, 1H), 6.95 (d, J=8.7 Hz, 2H), 7.08 (dd, J=8.4, 1.2 Hz, 1H), 7.25 (d, J=1.8 Hz, 1H), 7.74 (d, J=8.7 Hz, 2H), 8.14 (d, J=7.2 Hz, 1H); MS (ES) m/z: 579.1 (MH+); HRMS Calcd. for C26H35N4O9S(MH+): 579.1973. Found: 579.1955.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-0080e2a5dfaf483d93e7ba91f99ee65a
Source noteuspto-grants-2003_02