Methanol → Methyl 2-hydroxy-5-sulfamoylbenzoate

To 62 mmol 2-hydroxy-5-sulfamoyl-benzoic acid in 80 ml THF was added 80 mmol CDI and the mixture heated at 50° C. for 1 h. 616 mmol methanol was then added, and the mixture was heated at 50° C. for 16 h. The mixture was then cooled to room temperature, concentrated in vacuo, and the residue chromatographed on silica gel (eluant: dichloromethane/methanol 20:1). The product containing fractions were concentrated in vacuo and the residue suspended in ethyl acetate and washed with aq NaHCO3 solution. The organic phase was dried with Na2SO4 and concentrated in vacuo to afford the title compound. MS (m/e): 230.2 ([M−H]−, 100%)

1. temperaturethe mixture was heated at 50° C. for 16 h
2. temperatureThe mixture was then cooled to room temperature
3. concentrationconcentrated in vacuo
4. customthe residue chromatographed on silica gel (eluant: dichloromethane/methanol 20:1)
5. additionThe product containing fractions
6. concentrationwere concentrated in vacuo
7. washwashed with aq NaHCO3 solution
8. dry with materialThe organic phase was dried with Na2SO4
9. concentrationconcentrated in vacuo

ORD-Eintrag

ord-60b045a39ba14cd9aa06ad504ff2a7d7

Quelldatensatz

uspto-grants-2009_10

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07605163B2