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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298675Generated: October 31, 2026

2-Fluoro-4-biphenylboronic Acid → Methyl 4-[(3-fluoro-4-phenylphenyl)amino]-5-methylthiothiophene-2-carboxylate

https://huagongshe.com/reaction/2298675

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-4-biphenylboronic AcidHCID 2774698—
ReactantMethyl 4-amino-5-methylthiothiophene-2-carboxylateHCID 86583856—
ProductMethyl 4-[(3-fluoro-4-phenylphenyl)amino]-5-methylthiothiophene-2-carboxylateHCID 8675868941.6%

Reaction Steps

Using a procedure similar to Example 208, step (a), 74.4 mg (0.36 mmol) of methyl 4-amino-5-methylthiothiophene-2-carboxylate was allowed to react with 155.5 mg (2 equiv, 0.72 mmol) of 3-fluoro-4-phenylphenyl boronic acid to give 50.6 mg (41.6%) of methyl 4-[(3-fluoro-4-phenylphenyl)amino]-5-methylthiothiophene-2-carboxylate. 1H NMR (CDCl3, 400 MHz) δ2.44 (s, 3H), 3.91 (s, 3H), 6.19 (s, 1H), 6.78-6.86 (m, 2H), 7.32-7.39 (m, 2H), 7.73-7.47 (m, 2H), 7.55 (d, 1H, J=6.9 Hz), 7.82 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492403B1
Source datasetuspto-grants-2002_12
ORD IDord-b4993eb65f834b2f900d0440f763d127
Source noteuspto-grants-2002_12