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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121155Generated: November 2, 2026

Hydrochloric Acid → [4-Amino-2-(2-methylphenyl)benzoyl]methionine methyl ester hydrochloride

https://huagongshe.com/reaction/2121155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDichloromethaneHCID 6344—
Reactant[4-Nitro-2-(2-methylphenyl)benzoyl]methionine methyl esterHCID 53719134—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product[4-Amino-2-(2-methylphenyl)benzoyl]methionine methyl ester hydrochlorideHCID 6989264185%

Reaction Steps

[4-Nitro-2-(2-methylphenyl)benzoyl]methionine methyl ester was reduced to a corresponding amine by stannous chloride in ethyl acetate at 78° C. The free amine was treated with methylene chloride and 3 N HCl in ether to give [4-amino-2-(2-methylphenyl)benzoyl]methionine methyl ester hydrochloride (85% yield); [α]25D=−28.3 (c=1.0, methanol); 1H NMR (CD3OD) δ 7.74 (d, J=8.2 Hz, 1H), 7.47 (d, J=8.2 Hz, 1H), 7.23-7.30 (m, 5H), 4.47 (m, 1H), 3.69 (s, 3H), 2.06-2.18 (m, 4H), 1.99 (s, 3H), 1.97 (m, 2H), 1.74 (m, 1H); 13C NMR (CD3OD) δ 173.3, 170.8, 143.3, 139.7, 138.1, 137.2, 133.5, 131.49 130.8, 130.6, 129.6, 128.8, 126.2, 123.1, 66.9, 52.9, 31.5, 30.8, 20.4, 15.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693123B2
Source datasetuspto-grants-2004_02
ORD IDord-1db70ec99ecc437fac7f82676d2e4695
Source noteuspto-grants-2004_02