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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 2-Amino-6-bromonaphthalene | HCID 348404 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Bromo-6-(sulfamoylamino)naphthalene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07470807B2 |
|---|
| Source dataset | uspto-grants-2008_12 |
|---|
| ORD ID | ord-439009b9cbc64135ae37ed1c7f5f3d8d |
|---|
| Source note | uspto-grants-2008_12 |
|---|