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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412982Generated: October 29, 2026

1,1'-Biphenyl-4-yl-boronic acid → Methyl 4-[(4-phenylphenyl)amino]-5-methylthiothiophene-2-carboxylate

https://huagongshe.com/reaction/412982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-Biphenyl-4-yl-boronic acidHCID 151253—
ReactantMethyl 5-methylthio-4-[(4-phenylphenyl)amino]thiophene-2-carboxylateHCID 18537271—
ReactantMethyl 4-amino-5-methylthiothiophene-2-carboxylateHCID 86583856—
ProductMethyl 4-[(4-phenylphenyl)amino]-5-methylthiothiophene-2-carboxylateHCID 8658385719.1%

Reaction Steps

Methyl 5-methylthio-4-[(4-phenylphenyl)amino]thiophene-2-carboxylate: 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 142.5 mg (2 equiv, 0.72 mmol) of 4-phenylphenyl boronic acid to give 24.5 mg (19.1%) of methyl 4-[(4-phenylphenyl)amino]-5-methylthiothiophene-2-carboxylate. 1H NMR (CDCl3, 400 MHz) δ 2.45 (s, 3H), 3.92 (s, 3H), 6.38 (bs, 1H), 7.08-7.14 (m, 2H), 7.33 (m, 1H), 7.43-7.46 (m, 2H), 7.54-7.60 (m, 411), 7.82 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562840B1
Source datasetuspto-grants-2003_05
ORD IDord-ebd3e7c961764c3cb1b5805f9db4e89d
Source noteuspto-grants-2003_05