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Chemical Structure| 440125-30-4 Chemical Structure| 440125-30-4

Structure of 440125-30-4

Chemical Structure| 440125-30-4

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Product Details of [ 440125-30-4 ]

CAS No. :440125-30-4
Formula : C4H6N2O2
M.W : 114.10
SMILES Code : COCC1=NN=CO1

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Application In Synthesis of [ 440125-30-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 440125-30-4 ]

[ 440125-30-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 20605-41-8 ]
  • [ 122-51-0 ]
  • [ 440125-30-4 ]
YieldReaction ConditionsOperation in experiment
With toluene-4-sulfonic acid; at 140℃; for 8h; A mixture of above hydrazide (45 g), triethylorthoformate (146 mL) and p-toluenesulfonic acid (61mg) was heated at 140 °C for 8 h. Excess triethylorthoformate wasremoved under vacuum. The product was purified by silica gel column chromatography to yield4.6gof 2-methoxymethyl-l,3,4-oxadiazole.
toluene-4-sulfonic acid; at 140℃; for 8h; A mixture of above hydrazide (45 g), triethylorthoformate (146 mL) and p- toluenesulfonic acid (61mg) was heated at 140 C for 8 h. Excess triethylorthoformate was removed under vacuum. The product was purified by silica gel column chromatography to yield 4.6 g of2-methoxymethyl- [1. 3. 4] -oxadiazole.
With toluene-4-sulfonic acid; at 140℃; for 8h; Reference P Synthesis of [()-2-AMINO-1- (5-METHOXYMETHYL- [1,] 3,4] [OXADIAZOL-2-YL)-BUTAN-1-OL] Step 1 [(S)- (+)-2-AMINO-L-BUTANOL] (50 g, 561 mmol) in a mixture of water and dioxane (200 mL of water and: 200 mL) dioxane was cooled to [0 °C] and mixed with [NAOH] (26.9 g, 673 mmol) and di-tert-butyl-dicarbonate (146.96 g, 673 mmol). After the addition, the reaction was allowed to warm to room temperature. The reaction mixture was stirred for 2 h. After removing the dioxane, the residue was extracted with EtOAc, then washed with brine and dried with anhydrous [MGS04,] filtered and concentrated. Without further purification, the crude [(S)-2-BOC-AMINO-L-BUTANOL] (120 g) was used for next step reaction. Step 2 A solution of oxalyl chloride (40.39 g, 265 mmol) in [MECLZ] (700 mL) was stirred and cooled to-60 [°C.] Dimethylsulfoxide (51.7 g, 663 mmol) in [MECL2] (100 [ML)] was added dropwise. After 10 min. , a solution of [(S)-2-BOC-AMINO-L-BUTANOL] (50 g, 265 mmol) in [MECL2] (100 mL) was added dropwise [AT-70 °C.] The reaction mixture was allowed to warm to-40 °C for 10 min. and then cooled to-70 °C again. A solution of triethylamine (74.9 g, 742 mmol) in MeCl2 (100 mL) was added. The reaction mixture was allowed to warm to room temperature over 2 h. Saturated sodium dihydrogen phosphate (100 [ML)] was added, and then the organic layer was washed with brine and dried over [MGS04. THE] solvent was removed to yield 45g of [(S)-2-BOC-AMINO-BUTYRALDEHYDE (L-FORMYL-PROPYL)-CARBAMIC] acid [TERT-BUTYL] ester. Step 3 A mixture of methyl methoxyacetate (52 g, 500 mmol), hydrazine hydrate (30 mL) was heated to reflux for 8 h. Excess hydrazine and water were removed under vacuum. The residue was extracted with n-butanol, dried with [NA2SO4.] Excess n-butanol was removed to yield 45g of hydrazide. Step 4 A mixture of above hydrazide (45 g), [TRIETHYLORTHOFORMATE] (146 mL) and p- toluenesulfonic acid (61mg) was heated at [140 °C] for 8 h. Excess [TRIETHYLORTHOFORMATE] was removed under vacuum. The product was purified by silica gel column chromatography to yield 4.6g of 2-methoxymethyl-1, 3,4-oxadiazole. Step 5 To a stirred solution of 2-methoxymethyl-1, 3,4-oxadiazole (4.6 g, 40 mmol) in THF (100 mL) was added n-BuLi (1.6 M solution in 25.2 mL of hexane) dropwise under N2 at-78 [°C.] After 1 h, MgBr. Et2O (10.4 g, 40.3 mmol) was added and the reaction mixture was allowed to warm to-45 [°C] for 1 h before being treated with (S)-2-Boc-amino- propanylaldehyde butyraldehyde (5.28 g, 28.25 mmol) in THF (20 mL). The reaction mixture was stirred for 1 h, quenched with saturated [NH4C1,] and extracted with ethyl acetate. The organic layer was washed with brine, dried with MgS04 and concentrated. The residue was purified by silica gel column chromatography to yield [(S)-2-BOC-AMINO-1- (5-] methoxymethyl-[1, 3, [4]-OXADIAZOLE-2-YL)-1-PROPANOL] butanol (500 mg). Step 6 [2-BOC-AMINO-1- (5-METHOXYMETHYL- [1,] 3, [4]-OXADIAZOLE-2-YL)-1-PROPANOL] butanol (500 mg, 1.66 mmol), and MeCl2 (5 mL) were mixed and TFA (0.5 mL) was added at room temperature. After stirring for 1 h, the solvent and excess TFA were removed under vacuum to produce [(S)-2-AMINO-L- (5-METHOXYMETHYL- [1,] 3,4] oxadiazol-2-yl)-butan-1-ol. TFA salt (340 mg).
With toluene-4-sulfonic acid; at 140℃; for 8h; Step 4 A mixture of above hydrazide (45 g), triethylorthoformate (146 ml) andp-toluene- sulfonic acid (61mg) was heated at 140 °C for 8 h. Excess triethylorthoformate was removed under vacuum. The product was purified by silica gel column chromatography to yield 2- methoxymethyl- [1, 3, 4]-oxadiazole (4.6 g).

 

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