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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666913Generated: October 28, 2026

Hydrogen Peroxide → 6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid, 2-carboxy-4-(4-chlorophenyl)-3,9-dimethyl-, 6-methyl ester, (6S)-

https://huagongshe.com/reaction/1666913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium SulfiteHCID 24437—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
ReactantHCID 86639154HCID 86639154—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product6H-Thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine-6-acetic acid, 2-carboxy-4-(4-chlorophenyl)-3,9-dimethyl-, 6-methyl ester, (6S)-HCID 67446188126.4%

Reaction Steps

The compound (37.36 g) described in Example 1 and concentrated sulfuric acid (48.3 mL) were dissolved in acetic acid (32 mL). Acetic anhydride (189 mL) and manganese acetate (III) dihydrate (50.00 g) were successively added, and the mixture was stirred at room temperature for 1 hr. After completion of the reaction, water was added, and the mixture was extracted with ethyl acetate, and washed with 3N aqueous sodium hydroxide solution until the aqueous layer became pH 8. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated to give a brown oil (about 70 g). The obtained brown oil (about 70 g) was dissolved in methanol (300 mL). Sodium methoxide (81 g) was added, and the mixture was stirred at room temperature for 2 hr. After completion of the reaction, methanol was evaporated under reduced pressure. 1N hydrochloric acid (500 mL) was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated. The residue was purified by column chromatography (chloroform:methanol=97:3) to give methyl (S)-{4-(4-chlorophenyl)-2-hydroxymethyl-3,9-dimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl}acetate (19.85 g) and methyl (S)-{4-(4-chlorophenyl)-2-formyl-3,9-dimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl}acetate (4.82 g). The obtained methyl (S)-{4-(4-chlorophenyl)-2-formyl-3,9-dimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl}acetate (2.8 g) was dissolved in acetonitrile (20 mL), and aqueous sodium dihydrogen phosphate solution (640 mg/8 ml) was added. To the reaction mixture were successively added 35% hydrogen peroxide solution (3.2 mL) and aqueous sodium chlorite solution (1 g/2.8 ml) at 10° C., and the mixture was stirred for 1 hr on a water bath. After completion of the reaction, water was added, and the mixture was worked up with sodium sulfite. The aqueous layer was acidified and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated to give (S)-4-(4-chlorophenyl)-6-methoxycarbonylmethyl-3,9-dimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-2-carboxylic acid (3 g). The obtained (S)-4-(4-chlorophenyl)-6-methoxycarbonylmethyl-3,9-dimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-2-carboxylic acid (3.6 g) and copper (357 mg) were reacted at 150° C. for 15 min in quinoline (14 mL). After completion of the reaction, water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated. The residue was purified by column chromatography (chloroform:methanol=100:1) and recrystallized from hexane-ethyl acetate to give methyl (S)-{4-(4-chlorophenyl)-3,9-dimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl}acetate (821 mg). A mixture of the obtained methyl (S)-{4-(4-chlorophenyl)-3,9-dimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl}acetate (800 mg), dichlorobis(tricyclohexylphosphine)palladium (148 mg), bisneopentylglycolatodiboron (542 mg) and potassium acetate (294 mg) was stirred at 100° C. for 5 hr in dioxane (7 mL). After cooling, the mixture was partitioned by adding water and ethyl acetate. The organic layer was washed with saturated brine, and the solvent was evaporated. The residue was purified by column chromatography (chloroform:methanol=100:1) to give a boronic acid derivative (180 mg). To a mixture of the obtained boronic acid derivative (164 mg), dichlorobis(triphenylphosphine)palladium (II) (15 mg) and 5-bromonicotinonitrile (137 mg) were added 2 M aqueous sodium carbonate solution (1 mL) and tetrahydrofuran (1.6 mL), and the mixture was stirred at 100° C. for 4 hr. After cooling, water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated. The residue was purified by column chromatography (chloroform:methanol=100:1) and recrystallized from hexane-ethyl acetate to give the title compound (105 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044042B2
Source datasetuspto-grants-2011_10
ORD IDord-4ab50659e99146bdb5737ef30f844389
Source noteuspto-grants-2011_10