A kind of preparation method and application of iohexol intermediate impurity
A technology of an intermediate and iohexol, which is applied in the field of pharmaceutical synthesis and achieves the effects of short steps, simple preparation process and high purity
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Embodiment 1
[0057] The preparation of embodiment 1, formula 1 compound
[0058] The formula 2 compound (10g, 0.028mol) was added to the autoclave, followed by methanol (40g), acetic acid (25g) and Rh / C (1g), 5.5MPa H 2 After the reaction at room temperature, TLC monitored the completion of the reaction, suction filtration, and the filtrate was concentrated to dryness under reduced pressure at 40°C to obtain 8.6 g of the crude compound of formula 1. The weight yield of the crude product was 86%, and the purity was 87%.
Embodiment 2
[0059] Embodiment 2, the purification of formula 1 compound
[0060]Dissolve the compound of formula 1 (0.5g, 0.0014mol) in methanol (1ml), add silica gel (0.5g, 200-300 mesh) to mix the sample, 10g of silica gel (200-300 mesh) for column, first use 25mL ethyl acetate Elution, followed by elution with 85mL of ethyl acetate:methanol with a volume ratio of 1:1, and finally with 50mL of ethyl acetate:methanol:ammonia with a volume ratio of 1:2:0.01 for elution, TLC detection and collection , the product was concentrated to dryness under reduced pressure at 40°C to obtain 0.4 g of off-white solid, which was the pure compound of formula 1. The total molar yield is 85.8%, and the purity is 98%.
Embodiment 3
[0061] Embodiment 3, confirmation of the structure of the compound of formula 1 in embodiment 2
[0062] Mass Spectrum: ESI-MS(m / z): 334.1[M+H] +
[0063] High resolution mass spectrum: m / z: 334.1974[M+H] + ;Molecular formula: C14H27N3O6
[0064] Proton NMR spectrum: 1 HNMR(400MHz,DMSO-d6)δ7.72-7.70(t,2H),5.10-4.05(bs,4H),3.46-3.43(m,2H),3.27-3.22(m,4H),3.16-3.12( m,2H),2.98-2.93(m,2H),2.55-2.53(m,1H),2.23-2.19(t,2H),1.76-1.74(d,2H),1.63-1.60(m,1H), 1.37-1.41(m,1H),1.09-1.03(m,2H).
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