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Chemical Structure| 179167-09-0 Chemical Structure| 179167-09-0

Structure of 179167-09-0

Chemical Structure| 179167-09-0

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Product Details of [ 179167-09-0 ]

CAS No. :179167-09-0
Formula : C11H26N4O2
M.W : 246.35
SMILES Code : CC(C)(C)OC(=O)NCCN(CCN)CCN
MDL No. :MFCD18433376

Safety of [ 179167-09-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 179167-09-0 ]

* 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 [ 179167-09-0 ]

[ 179167-09-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6624-49-3 ]
  • [ 179167-09-0 ]
  • C31H36N6O4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
63.6% With 4-methyl-morpholine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; In N,N-dimethyl-formamide; at 50℃; for 12h; To a 250 ml eggplant flask was added <strong>[6624-49-3]isoquinoline-3-carboxylic acid</strong> (4) (415.2 mg, 2.4 mmol)Dissolved in DMF 30ml,N-t-butoxycarbonyltriaminoethylamine (5) (246.2 mg, 1 mmol)After dissolving in 5 ml DMFWas added dropwise to the flask, and then DMTMM (664.1 mg, 2.4 mmol) was added at an oil bath temperature of 50 C,After 12 h of reaction, the solvent was removed and then purified by column chromatography to give a white solid (353.6 mg, 63.6%).
61% With 4-methyl-morpholine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; In methanol; N,N-dimethyl-formamide; at 20℃; for 12h;pH 9;Inert atmosphere; A solution of 2 (519.0 mg, 3.0 mmol) and mono-N-Boc-protected TREN (3) (246.0 mg, 1.0 mmol) in DMF (50 mL) was prepared at room temperature under nitrogen. While stirring, DMTMM (4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholiniumchloride) (830.1 mg, 3 mmol) and NMM (N-methylmorpholine) were added (dropwise 2-3 ml) to get a pH of about 9. Then solution was diluted with methanol (10 ml) and allowed to stir at room temperature. After 12 h, the solvent was removed in vacuo and the residue was dissolved in ethyl acetate. After removal of solvent the crude product was purified by column chromatography using silica gel and CH2Cl2:MeOH (20:1). The product 4 (338.6 mg, 61%) was obtained as a white solid.
 

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