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ChemicalBook CAS DataBase List Methyl 5-acetaMido-2-aMino-4-ethoxybenzoate

Methyl 5-acetaMido-2-aMino-4-ethoxybenzoate synthesis

4synthesis methods
Methyl 5-acetaMido-4-ethoxy-2-nitrobenzoate

1201080-23-0
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Methyl 5-acetaMido-2-aMino-4-ethoxybenzoate

1222172-49-7
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Yield:1222172-49-7 91%

Reaction Conditions:

with hydrogen;Raney-Ni in tetrahydrofuran;methanol; for 3 h;

Steps:

3

Example 3 Methyl 4-ethoxy-5-acetylamido-2-aminobenzoate (a compound of formula II, R=methyl) The title compound of example 1 of methyl 4-ethoxy-5-acetylamido-2-nitrobenzoate (320 g, 1.13 mol) and Raney-Ni (40 g) were mixed with THF (1500 mL) and methanol (1500 mL) and stirred for 3 h under hydrogen. The reaction mixture was filtered, washed with dichloromethane, and the filtrate was distilled off the solvent to give 260 g of methyl 4-ethoxy-5-acetylamido-2-aminobenzoate with a yield of 91%. 1HNMR (300 MHz, DMSO-d6) δ 1.45 (t, 3H), 2.16 (s, 3H), 3.82 (s, 3H), 4.06 (q, 2H), 5.71 (br, 1H), 6.04 (s, 1H), 7.26 (s, 1H), 7.35 (br, 1H), 8.68 (s, 1H). MS/ESI: 252.9 (M+H).

References:

US2011/263860,2011,A1 Location in patent:Page/Page column 5

1201080-20-7 Synthesis
Benzoic acid, 3-(acetylamino)-4-ethoxy-, methyl ester

1201080-20-7
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Methyl 5-acetaMido-2-aMino-4-ethoxybenzoate

1222172-49-7
11 suppliers
inquiry