Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373159Generated: October 29, 2026

Chlorosulfamic acid → HCID 59850961, compound

https://huagongshe.com/reaction/2373159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfamic acidHCID 24499—
ReactantSodium hydrideHCID 24758—
ReactantHCID 59850926HCID 59850926—
SolventDimethylformamideHCID 6228—
ProductHCID 59850961HCID 59850961—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 95% NaH (0.017 g, 0.68 mmol) in DMF (2 mL) at 0° C. was added a solution of Compound 136 (0.10 g, 0.26 mmol) in DMF (2 mL) dropwise. The suspension was stirred at 0° C. for 1 h, then sulfamoyl chloride (0.067 g, 0.58 mmol) was added as a solid. After stirring for 1 h at 0° C., the mixture was treated with excess sulfamoyl chloride. After stirring overnight, the reaction was, quenched with water and extracted with EtOAc (3×5 mL). The combined organic phases were washed with brine, dried (Na2SO4), filtered and concentrated under reduced pressure at rt. The residue was purified by flash column chromatography (silica, 0-40% EtOAc/hexanes) to yield Compound 120 (0.1.0 g) as a white foam: HPLC: 4.12 min; MS (ES) m/z 461 (MH+); 1H NMR (DMSO-d6) δ 4.29-4.34 (m, 1H), 4.65-4.75 (m, 2H), 7.39-7.50 (m, 3H), 7.57-7.64 (m, 1H), 7.81-7.90 (m, 4H), 8.09 (d, 1H, J=8.5 Hz), 8.215 (d, 1H, J=2 Hz), 8.34 (s, 1H), 10.55 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459444B2
Source datasetuspto-grants-2008_12
ORD IDord-f4b875640cba457ba9d3c8ae789d2202
Source noteuspto-grants-2008_12