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Chemical Structure| 89180-90-5 Chemical Structure| 89180-90-5

Structure of 89180-90-5

Chemical Structure| 89180-90-5

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Product Details of [ 89180-90-5 ]

CAS No. :89180-90-5
Formula : C5H7ClN2
M.W : 130.58
SMILES Code : CN1C=NC=C1CCl
MDL No. :MFCD09055350
InChI Key :PECUDCBUFUGTTE-UHFFFAOYSA-N
Pubchem ID :14239695

Safety of [ 89180-90-5 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H315-H318-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340+P312-P305+P351+P338-P310-P332+P313-P362-P403+P233-P405-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 89180-90-5 ]

* 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 [ 89180-90-5 ]

[ 89180-90-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 38993-84-9 ]
  • [ 89180-90-5 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; In dichloromethane; (1 -Methyl- 1 H-imidazol-5-yl)methanol was converted to the corresponding alkyl chloride by reaction with thionyl chloride in DCM. N-[1 -(Fluoromethyl)cyclopropyl]-3- [(1 -methylpyrazol-4-yl)methyl]-2,4-dioxo-1 1H-quinazoline-6-sulfonamide (100 mg, 0.260 mmol), the alkyl chloride (37 mg, 0.286 mmol) and potassium carbonate (43 mg, 0.312 mmol) in DMF was conventionally heated to 70 °C for 4 h. Usual work-up afforded the desired product (37 mg, 0.074 mmol, 28percent) as an off-white powder.
With thionyl chloride;N,N-dimethyl-formamide; at 20℃; for 2h;Sonographic reaction; Thionyl chloride (3.88mL, 53.5mmol) was added dropwise to 3-methyl-3H-imidazol-4- yl)-methanol (o.3g, 2.68mmol). The reaction was sonicated briefly, treated with DMF (1 drop) and allowed to stir at ambident temperature for 1 h. The volatiles were removed and the residue treated with diethyl ether. The diethyl ether was decanted and the procedure repeated 3 times. The semi-solid residue was treated with dimethylamine in THF (6.69mL, 13.38mmol) followed DMF (1 mL). The reaction was heated in a CEM microwave reactor at 8O0C for 30 minutes, treated with acetic acid (1 ml_) and purified by SCX cartridge to give the title compound (0.18g, 1.22mmol). LC-MS (method 1): R, 2.9 min, m/z 140 [MH]+.
With thionyl chloride;N,N-dimethyl-formamide; for 0.5h; DMF (1 drop) was added to a slowly stirred solution of (3-methyl-3H-imidazol-4-yl)-methanol (11) (1.8 g, 16 mmol) dissolved in thionyl chloride (12 mL). After 30 minutes the solvent was removed under reduced pressure, and the resulting solid triturated with diethyl ether (20 mL). The resulting semi-solid was dried over night under vacuum, and used without further purification. 1H NMR (400 MHz, CI4-MQOR): delta 8.98 (s, IH), 7.63 (s, IH), 4.85 (s, 2H), 3.90 (s, 3H). 13C NMR (100 MHz, d4- MeOH): delta 138.3, 132.6, 120.5, 34.5, 33.9.
 

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