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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530672Generated: November 3, 2026

N-[6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl]methanesulfonamide → HCID 46932191, compound

https://huagongshe.com/reaction/530672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl]methanesulfonamideHCID 49758835—
ReactantHCID 66700053HCID 66700053—
ProductHCID 46932191HCID 46932191—

Reaction Conditions

Temperature90 °C

Reaction Steps

N-(3-bromo-5-tert-butyl-4-methoxyphenyl)acetamide (24 mg, 0.08 mmol) and N-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalene-2-yl)methanesulfonamide (64 mg, 0.18 mmol), were reacted in the same manner as Example 43 Part C, heating in an oil bath at 90° C. for 18 hours to give crude product which was purified on an Isco 4 g silica cartridge eluting with 5% methanol/chloroform to give the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 1.39 (s, 9H), 2.02 (s, 3H), 3.06 (s, 3H), 3.16 (s, 3H), 7.34-7.76 (m, 5H), 7.84-8.00 (m, 3H), 9.91 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353091B2
Source datasetuspto-grants-2016_05
ORD IDord-afbb837d2f8b4101b8667c234043ead7
Source noteuspto-grants-2016_05