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Chemical Structure| 1086375-50-9 Chemical Structure| 1086375-50-9

Structure of 1086375-50-9

Chemical Structure| 1086375-50-9

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Product Details of [ 1086375-50-9 ]

CAS No. :1086375-50-9
Formula : C7H5N3O2
M.W : 163.13
SMILES Code : O=C(C1=NC2=CC=NN2C=C1)O
MDL No. :MFCD09414725

Safety of [ 1086375-50-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 1086375-50-9 ]

* 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 [ 1086375-50-9 ]

[ 1086375-50-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1453176-67-4 ]
  • [ 1086375-50-9 ]
YieldReaction ConditionsOperation in experiment
87% With hydrogenchloride; acetic acid; In water; at 120.0℃; for 3.0h; Step 4 To a solution of methyl <strong>[1453176-67-4]pyrazolo[1,5-a]pyrimidine-5-carboxylic acid methyl ester</strong> ( 1 00 mg, 0.56 mmol, 1 .00 equiv) in acetic acid (5 mL) was added concentrated HCl (37%, 5 mL). The resulting solution was stirred for 3 h at 120 C, then concentrated under vacuum. The residue was dissolved in 3 mL of water and then adjusted to pH 5 with saturated aqueous sodium carbonate solution. The precipitated product was collected by filtration then air-dried to give 0.08 g (87%) of pyrazolo[1,5-a]pyrimidine-5-carboxylic acid as a light yellow solid. LC/MS (Method I, ESI): RT= 0.95 min, m/z = 164.0 [M+H]+
87% With hydrogenchloride; water; acetic acid; at 120.0℃; for 3.0h; Step 4 To a solution of methyl <strong>[1453176-67-4]pyrazolo[1,5-a]pyrimidine-5-carboxylic acid methyl ester</strong> ( 1 00 mg, 0.56 mmol, 1 .00 equiv) in acetic acid (5 mL) was added concentrated HC1 (37%, 5 mL). The resulting solution was stirred for 3 h at 120 C, then concentrated under vacuum. The residue was dissolved in 3 mL of water and then adjusted to pH 5 with saturated aqueous sodium carbonate solution. The precipitated product was collected by filtration then air-dried to give 0.08 g (87%) of pyrazolo[1,5-a]pyrimidine-5-carboxylic acid as a light yellow solid. LC/MS (Method I, ESI): RT= 0.95 min, m/z = 164.0 [M+H]+
87% With hydrogenchloride; acetic acid; In water; at 120.0℃; for 3.0h; Step 4 To a solution of methyl <strong>[1453176-67-4]pyrazolo[1,5-a]pyrimidine-5-carboxylic acid methyl ester</strong> ( 1 00 mg, 0.56 mmol, 1 .00 equiv) in acetic acid (5 mL) was added concentrated HCl (37%, 5 mL). The resulting solution was stirred for 3 h at 120 C, then concentrated under vacuum. The residue was dissolved in 3 mL of water and then adjusted to pH 5 with saturated aqueous sodium carbonate solution. The precipitated product was collected by filtration then air-dried to give 0.08 g (87%) of pyrazolo[1,5-a]pyrimidine-5-carboxylic acid as a light yellow solid. LC/MS (Method I, ESI): RT= 0.95 min, m/z = 164.0 [M+H]+
87% With hydrogenchloride; acetic acid; In water; at 120.0℃; for 3.0h; Intermediate 11: Pyrazolo [1,5-al pyrimidine-5-carboxylic acid [0212] Step 4. To a solution of methyl <strong>[1453176-67-4]pyrazolo[1,5-a]pyrimidine-5-carboxylic acid methyl ester</strong> (100 mg, 0.56 mmol, 1.00 equiv) in acetic acid (5 mL) was added concentrated HC1 (37%, 5 mL). The resulting solution was stirred for 3 h at 120 C, then concentrated under vacuum. The residue was dissolved in 3 mL of water and then adjusted to pH 5 with saturated aqueous sodium carbonate solution. The precipitated product was collected by filtration then air-dried to give 0.08 g (87%) of pyrazolo[1,5-a]pyrimidine-5-carboxylic acid as a light yellow solid. LC/MS (Method I, ESI): RT= 0.95 mi m/z = 164.0 [M+H].
87% With hydrogenchloride; acetic acid; In water; at 120.0℃; for 3.0h; [0220] Step 4. To a solution of methyl pyrazolo[l,5-a]pyrimidine-5-carboxylic acid methyl ester (100 mg, 0.56 mmol, 1.00 equiv) in acetic acid (5 mL) was added concentrated HC1 (37%, 5 mL). The resulting solution was stirred for 3 h at 120 C, then concentrated under vacuum. The residue was dissolved in 3 mL of water and then adjusted to pH 5 with saturated aqueous sodium carbonate solution. The precipitated product was collected by filtration then air-dried to give 0.08 g (87%) of pyrazolo[l,5-a]pyrimidine-5-carboxylic acid as a light yellow solid. LC/MS (Method I, ESI): RT= 0.95 min, m/z = 164.0 [M+H]+.

  • 2
  • [ 1086375-50-9 ]
  • [ 94341-56-7 ]
  • [ 1454284-63-9 ]
YieldReaction ConditionsOperation in experiment
42% With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20℃; for 3h; A solution of pyrazolo[1,5-a]pyrimidine-5-carboxylic acid (80 mg, 0.49 mmol, 1.00 equiv), <strong>[94341-56-7]4-benzenesulfonyl-benzylamine</strong> ( 130 mg, 0.53 mmol, 1 .07 equiv), HOBt (90 mg, 0.67 mmol, 1 .44 equiv), EDCI ( 1 10 mg, 0,57 mmol, 1 .44 equiv), and diisopropylethylamine (0.5 mL) in DMF (4 mL) was stirred for 3 h at rt. The resulting solution was diluted with 5 mL of water and the resulting solution was extracted with 3x20 mL of ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified on a silica gel column eluted with ethyl acetate/hexane (3: 1 ) to give 0.08 g (42%) of the title compound as an off-white solid. LC/MS (Method I, ESI): RT= 1 .72 min, m/z = 393.0 [M+H]+. 1H NMR (300 MHz, DMSO-d6) delta 9.62 (t, J = 6.3 Hz, 1 H), 9.21 (d, J = 6.3 Hz, 1 H), 8.33 (d, J = 2.4 Hz, 1 H), 7.86-7.89 (m, 4H), 7.47-7.66 (m, 6H), 6.84 (dd, = 2.4, 0.9 Etazeta, IotaEta), 4.49 (d, J = 6.3 Hz, 2H).
 

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