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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061327Generated: November 4, 2026

HCID 10523822, compound → HCID 10793825, compound

https://huagongshe.com/reaction/1061327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10523822HCID 10523822—
Reactant(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamideHCID 12047933—
ProductHCID 10793825HCID 10793825—

Reaction Steps

The title compound was prepared from (2S)-2-[4-(4-oxo-piperidine-1-yl)-benzoylamino]-3-phenyl-propionic acid methyl ester(which was obtained in Example 164) 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 180 as an off-white solid; mp >98° C. (decomposed); 1H NMR (300 MHz, DMSO-d6) δ 1.20-1.40 (m, 2H), 1.80-1.90 (m, 2H), 2.05-2.90 (m, 5H), 2.91 (s, 3H), 3.00-3.20 (m, 2H), 3.70-3.80 (m, 2H), 4.47 (dd, J=8.0, 4.3 Hz, 1H), 4.50-4.65 (m, 1H), 6.81 (d, J=8.2 Hz, 1H), 6.92 (d, J=8.9 Hz, 2H), 7.00 (dd, J=8.2, 2.0 Hz, 1H), 7.10-7.30 (m, 6H), 7.67 (d, J=8.9 Hz, 2H), 8.47 (d, J=7.8 Hz, 1H); MS (ES) m/z: 611.2 (MH+); HRMS Calcd. for C31H39N4O7S(MH+): 611.2534. Found: 611.2525.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-19c831caad79487181976ca259b9fd2a
Source noteuspto-grants-2003_02