(4-AMINO-PHENYL)-MORPHOLIN-4-YL-METHANONE
(4-AMINO-PHENYL)-MORPHOLIN-4-YL-METHANONE Basic information
- Product Name:
- (4-AMINO-PHENYL)-MORPHOLIN-4-YL-METHANONE
- Synonyms:
-
- CHEMBRDG-BB 3000462
- BUTTPARK 19\02-43
- ART-CHEM-BB B000462
- (4-AMINO-PHENYL)-MORPHOLIN-4-YL-METHANONE
- (4-AMINOPHENYL)(MORPHOLINO)METHANONE
- 4-AMINOBENZOIC ACID, MORPHOLIDE
- 4-(MORPHOLIN-4-YLCARBONYL)PHENYLAMINE
- AKOS B000462
- CAS:
- 51207-86-4
- MF:
- C11H14N2O2
- MW:
- 206.24
- Product Categories:
-
- Aromatics
- Heterocycles
- Intermediates & Fine Chemicals
- Pharmaceuticals
- Amines
- Mol File:
- 51207-86-4.mol
(4-AMINO-PHENYL)-MORPHOLIN-4-YL-METHANONE Chemical Properties
- Melting point:
- 132-135°C
- Boiling point:
- 426.9±40.0 °C(Predicted)
- Density
- 1.228±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- pka
- 3.43±0.10(Predicted)
- Appearance
- Off-white to light brown Solid
- CAS DataBase Reference
- 51207-86-4(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39
- HazardClass
- IRRITANT
- HS Code
- 2934999090
(4-AMINO-PHENYL)-MORPHOLIN-4-YL-METHANONE Usage And Synthesis
Uses
(4-Amino-Phenyl)-Morpholin-4-yl-Methanone is an morpholine derivative used in the preparation of tyrosine kinase inhibitors and other biologically active agents.
Synthesis
5397-76-2
51207-86-4
Step - (ii): Synthesis of (4-aminophenyl)(morpholino)methanone: Intermediate-8a (8.5 g, 35.9 mmol) was dissolved in methanol (200 mL), 10% Pd/C (850 mg) was added and stirred for 4 hours at room temperature under H2 atmosphere. After completion of the reaction, the reaction mixture was filtered through a diatomaceous earth pad and washed with excess methanol. The filtrate was concentrated in vacuum to afford the target product (7.0 g, 94.53%) as a light yellow solid.1H-NMR (400 MHz, DMSO-d6) δ: 7.12 (d, 2H, J = 8.4 Hz), 6.55 (d, 2H, J = 8.0 Hz), 5.5 (bs, 2H), 3.66-3.28 (m, 8H); MS (ES) m /z 207 (M + 1).
References
[1] Green Chemistry, 2018, vol. 20, # 1, p. 130 - 135
[2] Organic Letters, 2017, vol. 19, # 1, p. 194 - 197
[3] ACS Catalysis, 2015, vol. 5, # 3, p. 1526 - 1529
[4] Patent: WO2014/125410, 2014, A1. Location in patent: Page/Page column 26; 27
[5] Bioorganic and Medicinal Chemistry Letters, 2018, vol. 28, # 9, p. 1615 - 1620
(4-AMINO-PHENYL)-MORPHOLIN-4-YL-METHANONESupplier
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(4-AMINO-PHENYL)-MORPHOLIN-4-YL-METHANONE(51207-86-4)Related Product Information
- 3-chloro-4-(morpholin-4-ylcarbonyl)aniline
- (4-AMINO-PHENYL)-MORPHOLIN-4-YL-METHANONE
- MORPHOLINO(4-NITROPHENYL)METHANONE
- (4-AMINO-PHENYL)-(2,6-DIMETHYL-MORPHOLIN-4-YL)-METHANONE
- (2-AMINO-PHENYL)-MORPHOLIN-4-YL-METHANONE
- (3-AMINO-PHENYL)-MORPHOLIN-4-YL-METHANONE
- 1-[4-(MORPHOLINOCARBONYL)PHENYL]-2-PYRROLIDINONE
- (3-([(4-CHLOROPHENYL)SULFONYL]METHYL)-4-NITROPHENYL)(MORPHOLINO)METHANONE
- 2-methyl-4-(morpholin-4-ylcarbonyl)aniline
- 2-methyl-4-[(2-methylmorpholin-4-yl)carbonyl]aniline
- 3-chloro-4-[(2-methylmorpholin-4-yl)carbonyl]aniline
- 2,4,6-TRINITROBENZOIC MORPHOLIDE
- 3-chloro-4-[(2,6-dimethylmorpholin-4-yl)carbonyl]aniline
- TOSLAB 21963
- 4-[(2-methylmorpholin-4-yl)carbonyl]aniline
- 4-[4-(4-(PYRAZIN-2-YL)-1H-PYRAZOL-1-YL)BENZOYL]MORPHOLINE
- Morpholine, 4-(4-((2-(2-chlorophenyl)-6-methyl-4-pyrimidinyl)amino)ben zoyl)-, monohydrochloride
- TOSLAB 863386