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Chemical Structure| 110099-99-5 Chemical Structure| 110099-99-5

Structure of 110099-99-5

Chemical Structure| 110099-99-5

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Product Details of [ 110099-99-5 ]

CAS No. :110099-99-5
Formula : C5H2Cl2N2O
M.W : 176.99
SMILES Code : O=C(Cl)C1=CN=C(Cl)N=C1
MDL No. :MFCD09863165
InChI Key :JUYQWJULYXCBAV-UHFFFAOYSA-N
Pubchem ID :10631129

Safety of [ 110099-99-5 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P501-P260-P270-P264-P280-P303+P361+P353-P301+P330+P331-P363-P301+P312+P330-P304+P340+P310-P305+P351+P338+P310-P405
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 110099-99-5 ]

* 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 [ 110099-99-5 ]

[ 110099-99-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 38324-83-3 ]
  • [ 110099-99-5 ]
YieldReaction ConditionsOperation in experiment
With trichlorophosphate; at 80.0℃; for 16h; 2-(2-Chloro-pyrimidin-5-yl)-1-propyl-1H-benzoimidazole A suspension of <strong>[38324-83-3]2-hydroxy-pyrimidine-5-carboxylic acid</strong> (300 mg, 2.14 mmol) [J. Arukwe, K. Undheim, Acta. Chem. Scand. (1986) B40, 764-767], in POCl3 (20 ml) was heated to 80 C. for 16 h. The excess of POCl3 was evaporated and the residue was dried in HV for 2 h. The crude product was then taken up in anhydrous THF (30 ml), treated with N-propyl-benzene-1,2-diamine (354 mg, 2.36 mmol) and the solution was stirred for 1 h at RT. The mixture was then concentrated in vacuo. Purification by flash chromatography (100:0 to 75:25) afforded 2-(2-chloro-pyrimidin-5-yl)-1-propyl-1H-benzoimidazole (63 mg, 11%). UPLC (5-100% CH3CN): tR=0.974 min, MS (ES+): 273 [M+1].
With trichlorophosphate; at 80.0℃; for 48h; 7-Chloro-2-(2-chloro-pyrimidin-5-yl)-1-propyl-1H-benzoimidazole A suspension of <strong>[38324-83-3]2-hydroxy-pyrimidine-5-carboxylic acid</strong> (3.25 g, 23.2 mmol) [J. Arukwe, K. Undheim (1986) Acta. Chem. Scand., B40, 764-767], in POCl3 (100 ml) was heated to 80 C. for 48 h. The excess of POCl3 was evaporated and the residue was dried in HV for 2 h. The crude product was then taken up in anhydrous THF (30 ml), treated with 3-chloro-N-2-propyl-benzene-1,2-diamine (4.35 g, 23.6 mmol) and the solution was stirred for 20 h at RT. The mixture was then concentrated in vacuo. Purification by flash chromatography (DCM/MeOH 100:0 to 85:15) provided 7-chloro-2-(2-chloro-pyrimidin-5-yl)-1-propyl-1H-benzoimidazole (40% pure, 8.0 g, 46%). UPLC (5-100% CH3CN): tR=1.462 min, MS (ES+): 307 [M+1].
  • 2
  • [ 95928-49-7 ]
  • [ 110099-99-5 ]
 

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Related Functional Groups of
[ 110099-99-5 ]

Chlorides

Chemical Structure| 40929-48-4

A179568 [40929-48-4]

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Acyl Chlorides

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Related Parent Nucleus of
[ 110099-99-5 ]

Pyrimidines

Chemical Structure| 40929-48-4

A179568 [40929-48-4]

Pyrimidine-5-carbonyl chloride

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Chemical Structure| 933702-55-7

A217564 [933702-55-7]

2-Chloropyrimidine-5-carbaldehyde

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