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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378555Generated: October 25, 2026

Formic Acid → 2-Bromo-6-(sulfamoylamino)naphthalene

https://huagongshe.com/reaction/2378555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantEthyl AcetateHCID 8857—
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant2-Amino-6-bromonaphthaleneHCID 348404—
SolventBenzeneHCID 241—
Product2-Bromo-6-(sulfamoylamino)naphthaleneHCID 22559043—

Reaction Steps

A solution of chlorosulfonyl isocyanate (870 μl, WAKO) in benzene (10 ml) was added dropwise with formic acid (377 μl, WAKO) under ice cooling, warmed to room temperature, stirred and for 19.5 hours, then warmed to 40° C., and further stirred for 4 hours. The reaction mixture was added dropwise with a solution of 2-amino-6-bromonaphthalene (443 mg) in benzene (5 ml) under ice cooling, warmed to room temperature, and stirred 21.5 hours. The reaction mixture was filtered to obtain solid, and the solid was added with ethyl acetate, mixed and filtered again. The solvent of the filtrate was evaporated under reduced pressure. The residue was purified by column chromatography (Quad, hexane:ethyl acetate=2:1) to obtain the title compound (Intermediate 66, 158 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470807B2
Source datasetuspto-grants-2008_12
ORD IDord-439009b9cbc64135ae37ed1c7f5f3d8d
Source noteuspto-grants-2008_12