Simple exploration of 2-Amino-4-iodobenzoic acid

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 2-Amino-4-iodobenzoic acid, other downstream synthetic routes, hurry up and to see.

Adding a certain compound to certain chemical reactions, such as: 20776-54-9, name is 2-Amino-4-iodobenzoic acid, belongs to iodides-buliding-blocks compound, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound 20776-54-9, Computed Properties of C7H6INO2

Embodiment 19 2-amino-4-((4,4-dimethylthiochroman-6-yl)ethynyl)benzoic acid 6-Ethynyl-4,4-dimethylbenzothiopyran (405.6mg, 2mmol) and 2-amino-4-iodobenzoic acid (263mg, 1mmol) were added to a flask, followed by addition of Pd(PPh3)2Cl2 (42mg, 0.06mmol) and CuI (23mg, 0.12mmol). After the flask was purged with argon for 3 times to remove oxygen, 10mL dry DMF and 0.2mL dry Et3N were added via syringe. Then the reaction was continued at 75C for 12 h and monitored by TLC. After completion of the reaction, the reaction solution was cooled to room temperature and the reaction was quenched with saturated ammonium chloride solution. The mixture was diluted with ethyl acetate, washed with saturated ammonium chloride solution and saturated sodium chloride solution. The organic phase was dried over anhydrous sodium sulfate, filtered, concentrated and purified by flash column chromatography (PE:EtOAc = 5:1) to give WYC-212 (286mg, 85%). 1H NMR (500 MHz, CDCl3) delta 7.88 (d, J = 8.3 Hz, 1H), 7.52 (d, J = 1.7 Hz, 1H), 7.18 (dd, J = 8.1, 1.8 Hz, 1H), 7.06 (d, J = 8.1 Hz, 1H), 6.84 (d, J = 1.3 Hz, 1H), 6.81 (dd, J = 8.3, 1.5 Hz, 1H), 3.08 – 3.02 (m, 3H), 1.99 – 1.94 (m, 2H), 1.35 (s, 6H); 13C NMR (126 MHz, CDCl3) delta 165.25, 165.23, 163.21, 161.20, 142.29, 134.42, 133.26, 133.25, 131.70, 131.64, 129.97, 129.27, 126.75, 125.15, 125.12, 117.73, 117.05, 116.92, 116.66, 116.47, 98.04, 98.02, 81.71, 61.62, 37.29, 33.13, 30.09, 23.38, 14.42. ESI(+)-MS: 338.3 [M+1]+.

In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 2-Amino-4-iodobenzoic acid, other downstream synthetic routes, hurry up and to see.