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Chemical Structure| 63744-41-2 Chemical Structure| 63744-41-2

Structure of 63744-41-2

Chemical Structure| 63744-41-2

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Product Details of [ 63744-41-2 ]

CAS No. :63744-41-2
Formula : C6H4ClN3
M.W : 153.57
SMILES Code : ClC1=CN=CC2=NC=CN12
MDL No. :MFCD13193447
InChI Key :ORPGZTZXVOKJHD-UHFFFAOYSA-N
Pubchem ID :12841588

Safety of [ 63744-41-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 63744-41-2 ]

* 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 [ 63744-41-2 ]

[ 63744-41-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 7252-83-7 ]
  • [ 33332-28-4 ]
  • [ 63744-41-2 ]
YieldReaction ConditionsOperation in experiment
25.31% With hydrogen bromide; sodium hydrogencarbonate; In isopropyl alcohol;Reflux; Example 186Preparation of 1-Benzothiazol-6-yl-3-imidazo[1,2-a]pyrazin-5-yl-imidazolidin-2-one (186A) Synthesis of Intermediate 5-Chloro-imidazo[1,2-a]pyrazine (I-186a) NaHCO3 (4.215 g, 50.1736 mmol) and IPA (40 mL) were added to a mixture of 2-bromo-1,1-dimethoxy-ethane (6.37 mL, 10.8066 mmol), 40percent HBr (475 mL, 2.3157 mmol) and 2 drops of water previously refluxed for 1 hr. The reaction mixture was stirred for 5 mins and filtered. To the filtrate was added 6-chloro-pyrazin-2-ylamine (1 g, 7.7190 mmol) and the resulting mixture was refluxed for overnight. The reaction was monitored by TLC (50percent ethylacetate in hexane). The reaction mixture was neutralized with Na2CO3 and partitioned between ethylacetate and water. The organic layer was washed with water, brine, dried over Na2SO4 and concentrated. Purification by column chromatography on silica gel (1-2percent MeOH in CHCl3) afforded 300 mg of the product (25.31percent yield).1H NMR (400 MHz, CDCl3): delta 9.05 (s, 1H), 7.98 (s, 1H), 7.92-7.85 (m, 2H).LCMS: 97.85percent, m/z=154.0 (M+1)
25.31% NaI KX); (4.215g, 50.1736miotanol) and IPA (4OmL) were added to a mixture of 2- 0 brorno- 1.1 -dhneihoxs -ethane (6.37ml... I O.8066mmol), 40percent HBr (475mL. 2.3157mmol ) and 2 drops of water previously reUuxed tor I hr. The reaction mixture was stirred for 5mins and filtered. To the filtrate was added 6-chloro-pyra/in-2-ylamine (I g, 7.7190miotanol) and the resulting mixture was reflux ed for overnight. The reaction was monitored by TLC (50percent ethylacetate in hexane). The reaction mixture was neutrali/od 5 with Na2(X).; and partitioned between ethylacetate and water. The organic layer was washed with water, brine, dried over Na>SO; and concentrated. Purification by column ehromatograph) on silica gel ( 1-2percent McOH in CHC I4) afforded 30(.)mg of the product (25.31percent yield >.1H NMR (400 MIIz, CDCIj): 6 9.05 (s, I M). 7.98 (v IH), 7 92 -7.85 (m. 211).IX MS: 97.85percent. m// 154.0 (M .bul. 1)
  • 2
  • [ 107-20-0 ]
  • [ 33332-28-4 ]
  • [ 63744-41-2 ]
YieldReaction ConditionsOperation in experiment
73% In 1,2-dimethoxyethane; water; at 60℃; for 1.5h; To a solution of 6-chloropyrazin-2-amine (0.5 g, 3.86 mmol) in DME (3 mL) at room temperature was slowly added 2-chloroacetaldehyde (45percent aqueous solution, 2.4 mL, 14 mmol). The resulting mixture was heated to 66 °C for 90 minutes, cooled to room temperature, and then basified with IN NaOH. This basified mixture was extracted with EtOAc (2x). The combined organic layers were washed with brine, dried over sodium sulfate and concentrated. The crude material was purified by silica gel chromatography (eluting with 0-10percent MeOH in DCM) to provide Intermediate 59 (430 mg, 73percent yield). MS (ES): m/z= 153.9 [M+H]+. XH NMR (400 MHz, DMSO-d6) delta ppm 9.12 (1 H, s), 8.27 (1 H, s), 8.15 (1 H, s), 7.85 (1 H, s). Intermediate 59 was used in the synthesis of Example 251.
 

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