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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061421Generated: October 30, 2026

(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamide → HCID 86584577, compound

https://huagongshe.com/reaction/1061421

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamideHCID 12047933—
ReactantHCID 86584575HCID 86584575—
ProductHCID 86584577HCID 86584577—

Reaction Steps

The title compound was prepared from ethyl ({[butyl-4-(4-oxo-1-piperidineyl)anilino]carbonyl}amino)acetate (which was obtained in Example 367) 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 278 as a white solid; 1H NMR (300 MHz, DMSO-d6) δ 0.83 (t, J=7.1 Hz, 3H), 1.17 (t, J=7.1 Hz, 3H), 1.15-1.40 (m, 6H), 1.80-1.95 (m, 2H), 2.50-2.80 (m, 5H), 2.90 (s, 3H), 3.49 (t, J=6.9 Hz, 2H), 3.55-3.60 (m, 2H), 3.65 (d, J=5.9 Hz, 2H), 4.04 (q, J=7.1 Hz, 2H), 4.48 (dd, J=7.9, 4.4 Hz, 1H), 5.60 (t, J=5.9 Hz, 1H), 6.80 (d, J=8.2 Hz, 1H), 6.90-7.10 (m, 5H), 7.17 (d, J=2.0 Hz, 1H); MS (ES) m/z: 606.3 (MH+); HRMS Calcd. for C29H44N5O7S(MH+): 606.2956. Found: 606.2955.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-3d7f38a64b134d9aba95e7ff87c52424
Source noteuspto-grants-2003_02