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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061261Generated: November 4, 2026

(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamide → HCID 69654906, compound

https://huagongshe.com/reaction/1061261

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamideHCID 12047933—
ReactantHCID 86588908HCID 86588908—
ProductHCID 69654906HCID 69654906—

Reaction Steps

The title compound was prepared from ethyl{5-[4-(1,4-dioxa-8-azaspiro[4.5]dec-8-yl)phenyl]-2H-tetraazol-2-yl}acetate (which was obtained in Example 48) and N-[5-((1R)-2-amino-1-hydroxy-ethyl)-2-hydroxy-phenyl]-methanesulfonamide (which was obtained in Example 10) according to the procedures of Example 98 and Example 99 as a white solid; mp >240° C. (decomposed); 1H NMR (300 MHz, DMSO-d6) δ 1.45-1.65 (m, 2H), 1.90-2.10 (m, 2H), 2.50-3.10 (m, 5H), 2.95 (s, 3H), 3.65-3.85 (m, 2H), 4.89 (brd, J=8.3 Hz, 1H), 5.08 (d, J=15.9 Hz, 1H), 5.15 (d, J=15.9 Hz, 1H), 6.88 (d, J=8.3 Hz, 1H), 6.95 (d, J=8.7 Hz, 2H), 7.09 (dd, J=8.3, 2.0 Hz, 1H), 7.26 (d, J=2.0 Hz, 1H), 7.87 (d, J=8.7 Hz, 2H); MS (ES) m/z: 532.1 (MH+); HRMS Calcd. for C21H30N7O4S(MH+): 532.1973. Found: 532.1965.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-ecace6ecde9a457c876671232fd4444f
Source noteuspto-grants-2003_02