Details
Quality manufacturer supply Naftifine 65472-88-0 in stock with high standard
- Molecular Formula: C21H21N
- Molecular Weight: 287.404
- Vapor Pressure: 6.07E-08mmHg at 25°C
- Melting Point: 177 °C
- Boiling Point: 440.1 °C at 760 mmHg
- PKA: 7.99±0.50(Predicted)
- Flash Point: 194.4 °C
- PSA: 3.24000
- Density: 1.082 g/cm3
- LogP: 5.78700
Naftifine(Cas 65472-88-0) Usage
|
Indications |
Naftifine (Naftin) is a synthetic allylamine derivative topical antifungal agent that works by blocking squalene 2,3-epoxidase, resulting in increased cell membrane permeability and cell death. It is structurally and pharmacologically related to terbinafine. It also has some antiinflammatory properties that may be due to its ability to alter chemotaxis by polymorphonucleocytes. It is most effective against dermatophytes, moderately active against molds, and less active against yeasts, including C. albicans. |
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Manufacturing Process |
To a mixture of 1.42 g of methyl-(1-naphthylmethyl)amine hydrochloride, 2.89 g of sodium carbonate and 10 ml of dimethylformamide is added, at room temperature, 1.25 g of cinnamyl chloride, dropwise. After 18 hours stirring, at room temperature, the mixture is filtered and the filtrate is evaporated in vacuo. The residue is dissolved in toluene and, after drying over sodium sulphate, evaporated to obtain the trans-N-(cinnamylmethyl)-Nmethyl-(1-naphthylmethyl)amine compound, boiling point 162-167°C/0.015 Torr.The free base may be converted, with isopropanolic hydrogen chloride solution, into the hydrochloride form, melting point 177°C (from propanol). |
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Therapeutic Function |
Antifungal |
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Synthesis Reference(s) |
Journal of Medicinal Chemistry, 29, p. 112, 1986 DOI: 10.1021/jm00151a019Tetrahedron Letters, 25, p. 2535, 1984 DOI: 10.1016/S0040-4039(01)81224-7 |
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Pharmaceutical Applications |
A topical antifungal used as a 1% cream for the treatment of dermatophytoses, including tinea pedis, tinea corporis and tinea cruris. |
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Synthesis |
Naftifine, (E)-N-methyl-N-(3-phenyl-2-propenyl)-1-naphthalinmethanamine (35.3.1), is synthesized by alkylating N-methyl-(1-naphthylmethyl)-amine with cinnamyl chloride in the presence of sodium carbonate. |
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Definition |
ChEBI: A tertiary amine in which the nitrogen is substituted by methyl, alpha-naphthylmethyl, and (1E)-cinnamyl groups. It is used (usually as its hydrochloride salt) for the treatment of fungal skin infections. |
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Brand name |
Naftin (Merz). |
InChI:InChI=1/C21H21N.ClH/c1-22(16-8-11-18-9-3-2-4-10-18)17-20-14-7-13-19-12-5-6-15-21(19)20;/h2-15H,16-17H2,1H3;1H/b11-8+;
65472-88-0 Relevant articles
THE BORONIC ACID MANNICH REACTION: A NEW METHOD FOR THE SYNTHESIS OF GEOMETRICALLY PURE ALLYLAMINES
Petasis, Nicos A.,Akritopoulou, Irini
, p. 583 - 586 (1993)
Reaction of vinyl boronic acids with the...
Preparation method for synthesizing amine compound through co-catalysis and hydrosilylation of amide by iridium and boron reagents
-
Paragraph 0035-0038, (2022/04/03)
The invention relates to a preparation m...
Amine compound as well as preparation method and application thereof
-
Paragraph 0077; 0083-0086, (2021/08/21)
The invention discloses an amine compoun...
Oxidative Rearrangement of MIDA (N-Methyliminodiacetic Acid) Boronates: Mechanistic Insights and Synthetic Applications
Kaldas, Sherif J.,Tien, Chieh-Hung,Gomes, Gabriel Dos Passos,Meyer, Stephanie,Sirvinskas, Martynas,Foy, Hayden,Dudding, Travis,Yudin, Andrei K.
supporting information, p. 324 - 328 (2021/01/26)
Herein we report that coordinative hemil...
N -Butylpyrrolidone (NBP) as a non-toxic substitute for NMP in iron-catalyzed C(sp2)-C(sp3) cross-coupling of aryl chlorides
Bisz, Elwira,Koston, Martina,Szostak, Michal
supporting information, p. 7515 - 7521 (2021/10/12)
Although iron catalyzed cross-coupling r...
65472-88-0 Process route
-
-
98977-94-7
(±)-3-(N-methyl-N-((naphthalen-5-yl)methyl)amino)-1-phenylpropan-1-ol
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65472-88-0
naftifine
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride;
In
water;
Reflux;
|
90%
|
|
With
hydrogenchloride;
for 2h;
Heating;
|
-
-
N-cinnamyl-N-methyl-1-naphthylamide
-
-
65472-88-0
naftifine
| Conditions | Yield |
|---|---|
|
With
lithium aluminium tetrahydride;
In
diethyl ether;
at 0 ℃;
Reflux;
Inert atmosphere;
|
89%
|
65472-88-0 Upstream products
-
50-00-0
formaldehyd
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6783-05-7
trans-2-phenylvinylboronic acid
-
14489-75-9
N-methyl-1-naphthalenemethylamine
-
92610-10-1
(E)-N-(naphthalen-1-ylmethyl)-3-phenylprop-2-en-1-amine
65472-88-0 Downstream products
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98977-55-0
N-methyl-N-(3-phenylpropyl)-1-naphthalenemethanamine
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