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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729977Generated: October 30, 2026

Formic Acid → HCID 57833459, compound

https://huagongshe.com/reaction/729977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantChlorosulfamic acidHCID 24499—
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantHCID 136183339HCID 136183339—
SolventMethanolHCID 887—
SolventDimethylacetamideHCID 31374—
ProductHCID 57833459HCID 57833459—

Reaction Steps

To neat chlorosulfonyl isocyanate (0.166 g, 1.37 mmol) was added dropwise formic acid (97%, 0.63 g, 1.37 mmol) while cooling in ice-water bath. The mixture was stirred at rt until gas evolution ceased. The resulting sulfamoyl chloride was added to a solution of 4-{2-amino-6-[(4-{[2-(trifluoromethyl)pyridin-4-yl]oxy}phenyl) amino] pyrimidin-4-yl} phenol (0.06 g, 0.14 mmol, Example 51) in dry N,N-dimethylacetamide at 0° C. The reaction mixture was then stirred at rt for 12 h. The solution was diluted with methanol and separated by preparative HPLC. The desired fractions were combined, basified with saturated sodium carbonate, and extracted with EtOAc (3×). The extracts were combined, washed with brine, dried over magnesium sulfate, and evaporated to give desired product, 0.025 g (35%). 1H NMR (DMSO-d6) δ 9.42 (s, 1H), 8.59 (d, 1H), 8.09 (d, 2H), 7.98 (m, 2H), 7.85 (m, 2H), 7.35 (m, 3H), 7.10 (m, 3H), 6.42 (s, 1H), 6.36 (s, 2H); MS ES 519 (M+H)+calcd 519.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582646B2
Source datasetuspto-grants-2009_09
ORD IDord-0b9892ade7ff49dd9db46018f8d29076
Source noteuspto-grants-2009_09