ethyl 4-[(2-amino-4-chlorophenyl)amino]piperidine-1-carboxylate
ethyl 4-[(2-amino-4-chlorophenyl)amino]piperidine-1-carboxylate Basic information
- Product Name:
- ethyl 4-[(2-amino-4-chlorophenyl)amino]piperidine-1-carboxylate
- Synonyms:
-
- Domperidone Impurity 2
- ethyl 4-((2-amino-4-chlorophenyl)
- ethyl 4-[(2-amino-4-chlorophenyl)amino]piperidine-1-carboxylate
- ETHYL 4-(2-AMINO-4-CHLOROANILINO)PIPERIDINE-1-CARBOXYLATE
- 4-[(2-Amino-4-chlorophenyl)amino]-1-piperidinecarboxylic acid ethyl ester
- Einecs 258-775-8
- 1-PIPERIDINECARBOXYLIC ACID,4-[(2-AMINO-4-CHLOROPHENYL)AMINO]-,ETHYL ESTER
- Domperidone Impurity 8
- CAS:
- 53786-45-1
- MF:
- C14H20ClN3O2
- MW:
- 297.78
- EINECS:
- 258-775-8
- Mol File:
- 53786-45-1.mol
ethyl 4-[(2-amino-4-chlorophenyl)amino]piperidine-1-carboxylate Chemical Properties
- Boiling point:
- 475.6±45.0 °C(Predicted)
- Density
- 1.290±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- pka
- 4.70±0.11(Predicted)
- InChI
- InChI=1S/C14H20ClN3O2/c1-2-20-14(19)18-7-5-11(6-8-18)17-13-4-3-10(15)9-12(13)16/h3-4,9,11,17H,2,5-8,16H2,1H3
- InChIKey
- PPCPQDDCMQRJLS-UHFFFAOYSA-N
- SMILES
- N1(C(OCC)=O)CCC(NC2=CC=C(Cl)C=C2N)CC1
ethyl 4-[(2-amino-4-chlorophenyl)amino]piperidine-1-carboxylate Usage And Synthesis
Uses
Ethyl 4-((2-Amino-4-chlorophenyl)amino)piperidine-1-carboxylate is an impurity of Domperidone(D531100); a novel peripheral dopamine receptor antagonist that does not cross the blood-brain barrier; anti-emetic. Domperidone(Motilium) is a dopamine blocker and an antidopaminergic reagent.
Synthesis
53786-44-0
53786-45-1
2. 1.34 kg of the crude product (domperidone impurity 7) obtained in the first step was dissolved in a solvent mixture of 15 L of methanol and 15 L of tetrahydrofuran with 1.3 L of water. Subsequently, zinc powder and 1.1 kg of ammonium chloride were added and the reaction was carried out at 25 °C for 5 hours. After completion of the reaction, the zinc powder was removed by filtration. Methanol and tetrahydrofuran were recovered by concentration under reduced pressure. The residue was dissolved in 15 L of ethyl acetate and the organic phase was washed with 15 L of water. The organic phase was recrystallized by adding 1 kg of ethyl acetate and 3 kg of petroleum ether to give 1.06 kg of an off-white solid, domperidone intermediate (DP-2), with 99% purity and 88% yield.
References
[1] Journal of Medicinal Chemistry, 1987, vol. 30, # 5, p. 814 - 820
[2] Bioorganic and Medicinal Chemistry Letters, 2006, vol. 16, # 19, p. 5052 - 5056
[3] Patent: US4470989, 1984, A
[4] Patent: CN108358832, 2018, A. Location in patent: Paragraph 0007; 0020; 0023; 0029; 0033; 0037
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ethyl 4-[(2-amino-4-chlorophenyl)amino]piperidine-1-carboxylate(53786-45-1)Related Product Information
- ethyl 4-[(4-chloro-2-nitrophenyl)amino]piperidine-1-carboxylate
- 1-(3-Chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one
- 5-Chloro-1-(4-piperidyl)-2-benzimidazolinone
- 1-PIPERIDINECARBOXYLIC ACID, 4-[(4-AMINO-5-CHLOROPHENYL)AMINO], ETHYL ESTER
- 1-(3-BroMopropyl)-1,3-dihydro-2H-benziMidazol-2-one
- 1-(3-chloropropyl)-1,3-dihydro-3-(1-methylvinyl)-2H-benzimidazol-2-one
- Domperidone Impurity 15
- DoMperidone-d6
- DoMperidone EP IMpurity B
- TERT-BUTYL 4-[4-(AMINOMETHYL)PHENYL]TETRAHYDRO-1(2H)-PYRAZINECARBOXYLATE
- METHYL 4-[(4-METHYLPIPERAZIN-1-YL)METHYL]BENZOATE
- 4-((4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)Methyl)benzonitrile
- Oxazole, 4-[4-(trifluoromethyl)phenyl]-
- 4-(4-METHYLPIPERAZIN-1-YLMETHYL)BENZONITRILE
- 4-[[1-(TERT-BUTOXYCARBONYL)-4-PIPERIDINYL]OXY]BENZOIC ACID
- 1-(2-PROPENYL)-2-BENZIMIDAZOLIDINONE
- DoMperidone EP IMpurity D
- 2H-Benzimidazol-2-one, 1,1'-(1,3-propanediyl)bis[1,3-dihydro-