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Chemical Structure| 170985-85-0 Chemical Structure| 170985-85-0

Structure of 170985-85-0

Chemical Structure| 170985-85-0

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Product Details of [ 170985-85-0 ]

CAS No. :170985-85-0
Formula : C13H20N2O2
M.W : 236.31
SMILES Code : O=CNN[C@@H](CC)[C@@H](OCC1=CC=CC=C1)C
MDL No. :MFCD11977289

Safety of [ 170985-85-0 ]

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

Application In Synthesis of [ 170985-85-0 ]

* 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 [ 170985-85-0 ]

[ 170985-85-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 184177-81-9 ]
  • [ 170985-85-0 ]
  • [ 184177-83-1 ]
YieldReaction ConditionsOperation in experiment
70% With triethylamine; In 1,4-dioxane; at 90 - 100℃; for 24h; mixture of N?-((2S,3S)-2-(benzyloxy)pentan-3-yl)formohydrazide compound of formula-17 (45.5 g) obtained in example-13, dioxane (500 ml) added <strong>[184177-81-9]phenyl 4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenylcarbamate</strong> compound of formula-19 (50 g) was heated to 90-100 C. Triethylamine (26 g) was added to the reaction mixture at 90-100 C. over a period of 1 hour and stirred for 24 hours at 90-100 C. After completion of the reaction, the reaction mixture was cooled to 25-30 C. and dichloromethane was added to the reaction mixture. Filtered the reaction mixture through hyflow bed and washed with dichloromethane. Water was added to the filtrate. Both organic and aqueous layers were separated and the aqueous layer was extracted with dichloromethane. Both organic layers were combined and washed with 2% sodium hydroxide solution followed by water, and then with 5% hydrochloric acid solution followed by water and 5% NaHCO3 solution washing. Distilled off the solvent from organic layer under reduced pressure to get the title compound. Isopropyl alcohol (75 ml) was added to the obtained compound and the reaction mixture was cooled to 25-30 C. The reaction mixture was stirred for 6 hours at 25-30 C. Filtered the solid, washed with isopropyl alcohol and then dried to get the title compound. Yield: 28 g; Purity by HPLC: 97.67%; Impurity-A: 0.37%b) Purification of Compound of Formula-20 The obtained compound of formula-20 (30 g) was dissolved in methanol (960 ml) by heating at 60-65 C. The reaction mixture was cooled to 25-30 C. and stirred for 30 minutes at the same temperature. Filtered the precipitated solid and dried to get the pure compound of formula-20. Yield: 70%; Purity by HPLC: 99.15%; Impurity-A: 0.09%
0.89 kg With triethylamine; In 1,4-dioxane; at 90 - 95℃;Large scale; N'-[(l S,2S)-2-(Benzyloxy)-l-ethylpropyl]formic hydrazide (1 kg) and 1,4- Dioxane (5 lit) were added to the flask at room temperature along with Phenyl 4- (4-(4-hydroxyphenyl)piperazin-l-yl)phenylcarbamate (1.4 kg). The reaction mass was heated to 90-95C and Triethylamine (0.89 lit) was slowly added and stirred for 1 hr and maintained for 12-18 hrs. TLC was checked for intermediate and cooled to Room temperature and Dichloromethane (20 lit) was charged and filter through the Hyflow bed and washed with Dichloromethane (5 lit). Water (4 lit) was added and stirred for 10 min. Aqueous layer and Organic layer were separated and organic layer was washed with brine solution. Organic layer was separated and dried with Sodium sulphate and distilled completely under vacuum at below 50C and co- distilled with Toluene (1 lit) and Isopropyl alcohol (1 lit). Isopropyl alcohol (2.5 lit) was added to the crude and maintained at 65-70C for 1 hr, then cooled to Room temperature, stirred for 30 min and cooled to 10-15C, and then filtered and washed with Isopropyl alcohol (0.5 lit).Out Put: 0.89 kg; HPLC: 97%.
With triethylamine; In 1,4-dioxane; at 90 - 100℃; for 24h; A mixture of compounds 4 (18.0 g, 0.046 mol), 5 (16.38 g, 0.069 mol), and dioxane (180 mL) was heated to 90-100 C. Triethylamine (9.36 g, 0.092 mol) was added to the reaction mixture and then stirred for 24 h at 90-100 C. After the completion of the reaction, the reaction mixture was cooled to 25-30 C and dichloromethane (25 mL) was added to the reaction mixture. Compound 1 was obtained by filtration and concentration under vacuo and stirred in isopropyl alcohol (27 mL) at 25-30 C for 6 h. Pure compound 1 was got by recrystallization with methanol. 1H NMR (DMSO-d6, 400 MHz): delta 0.793 (t, 3H, CH3), 1.242 (d, 3H, CH3), 1.765 (q, 2H, CH2), 3.122 (t, 4H, piperazine-CH2), 3.327 (t, 4H, piperazine-CH2), 3.745 (m, 1H, N-CH), 3.990 (m, 1H, O-CH), 4.275-4.544 (d, 2H, Ar-CH2), 6.691 (d, 2H, Ar-H), 6.869 (d, 2H, Ar-H), 7.119 (d, 2H, Ar-H), 7.172 (q, 2H, Ar-H), 7.232 (m, 3H, Ar-H), 7.476 (d, 2H, Ar-H), 8.323 (s, 1H, N2C-H), 8.787 (s, 1H, Ar-OH). HRMS (ESI+): m/z: calcd for C30H35N5O3: 536.2638 [M+Na+]; found: 536.2619. IR (KBr, lambda, cm-1): 3468.1 (s), 1678.2 (s), 1605.1 (m), 1485.07 (s), 1231.9 (s), 1115.4 (s).
 

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