ChemicalBook--->CAS DataBase List--->106685-41-0

106685-41-0

106685-41-0 Structure

106685-41-0 Structure
IdentificationBack Directory
[Name]

Mehtyl 6-[3-(1-adamanty)-4-methoxy phenyl]-2-naphthoate
[CAS]

106685-41-0
[Synonyms]

Adap-int C
Adapalene IMpurity E
Mehtyl 6-[3-(1-adama
Adapalene Impurity 5
Adapalene Impurity 6
Adapalene Methyl Ester
Adapalene Related CoMpound B
Adapalene USP Related Compound B
Mehtyl 6-[3-(1-adamanty)-4-methoxy
Methyl 6-[3-(1-Adamantyl)-4-methoxy
6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthoate
Methyl6-[3-(1-adamanty)-4-methoxyphenyl]-2-naphthoate
METHYL 6-[3-(1-ADAMANTYL)-4-METHOXYPHENYL]-2-NAPHTHOATE
Mehtyl 6-[3-(1-adamanty)-4-methoxy phenyl]-2-naphthoate
METYL 6-[3-(1-ADAMANTYL)-4-METHOXY PHENYL]-2-NAPHTHOATE
Mehtyl 6-[3-(1-adamantyl)-4-methoxy phenyl]-2-naphthoate
6-[3-(1-Adamantyl-4-methoxyphenyl]-2-naphthatemethylester
Methyl 6-(3-(adaMantan-1-yl)-4-Methoxyphenyl)-2-naphthoate
Mehtyl 6-[3-(1-adamanty)-4-methoxy phenyl]-2-naphthoate(Adapalene)
Methyl 6-[3-(1-AdaMantyl)-4-Methoxyphenyl]-2-naphthalenecarboxylate
6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthalenecarboxylic acid methyl ester
Adapalene Related Compound B (50 mg) (Methyl 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthoate)
2-Naphthalenecarboxylic acid, 6-(4-methoxy-3-tricyclo[3.3.1.13,7]dec-1-ylphenyl)-, methyl ester
[EINECS(EC#)]

808-698-6
[Molecular Formula]

C29H30O3
[MDL Number]

MFCD08063923
[MOL File]

106685-41-0.mol
[Molecular Weight]

426.55
Chemical PropertiesBack Directory
[Melting point ]

223-225°C
[Boiling point ]

589.6±50.0 °C(Predicted)
[density ]

1.185±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform (Slightly)
[form ]

neat
[color ]

White to Off-White
[Major Application]

pharmaceutical (small molecule)
[InChI]

1S/C29H30O3/c1-31-27-8-7-24(14-26(27)29-15-18-9-19(16-29)11-20(10-18)17-29)22-3-4-23-13-25(28(30)32-2)6-5-21(23)12-22/h3-8,12-14,18-20H,9-11,15-17H2,1-2H3
[InChIKey]

PGXNMQBGOVUZNC-UHFFFAOYSA-N
[SMILES]

O(C)c1c(cc(cc1)c5cc6c(cc(cc6)C(=O)OC)cc5)C32CC4CC(C3)CC(C2)C4
Safety DataBack Directory
[Symbol(GHS) ]

Health Hazard (GHS08)
GHS08
[Signal word ]

Warning
[Hazard statements ]

H361d
[Precautionary statements ]

P201-P202-P280-P308+P313-P405-P501
[Hazard Codes ]

Xi
[Risk Statements ]

36/38
[Safety Statements ]

26
[WGK Germany ]

WGK 3
[REACH Registrations]

Inactive
[HS Code ]

2918992090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Repr. 2
Hazard InformationBack Directory
[Chemical Properties]

White to Off-White Solid
[Uses]

Adapalene intermediate
[Synthesis]

Methyl 6-bromo-2-naphthoate

33626-98-1

1-(5-Bromo-2-methoxy-phenyl)adamantane

104224-63-7

Mehtyl 6-[3-(1-adamanty)-4-methoxy phenyl]-2-naphthoate

106685-41-0

General procedure for the preparation of methyl 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-naphthalenecarboxylate (V): magnesium scraps (1.26 g, 51.85 mmol) were mixed with THF (10 mL) under nitrogen protection and stirred at room temperature. 2-(1-adamantyl)-4-bromoanisole (IV) (1.4 g, 4.36 mmol) and 1,2-dibromoethane (0.56 mL) were added, and the reaction mixture was subsequently heated to 40 °C to initiate the reaction. Then a solution of 2-(1-adamantyl)-4-bromoanisole (12.6 g, 39.25 mmol) in THF (40 mL) was slowly added dropwise under reflux conditions for 30 min. A solution of purified zinc chloride (8.4 g, 61 mmol) in THF (30 mL) was added slowly dropwise at reflux temperature over 15 minutes. After the reaction mixture was refluxed for 1 h, methyl 6-bromo-2-naphthalenecarboxylate (8.0 g, 30 mmol) was added and stirred for 10 min, followed by the addition of NiCl2ZDPPE catalyst (0.21 g). The mixture was continued to be stirred at the same temperature for 2 h. The residue was subsequently concentrated. The residue was treated with dichloromethane (100 mL) and 1N HCl (100 mL), and the dichloromethane layer was washed sequentially with 10% EDTA disodium salt solution and water, dried with anhydrous sodium sulfate, and distilled to give the crude product. The crude product was stirred in ethyl acetate (140 mL) at 70 °C for 1 h, cooled to 15 °C and kept for 1 h. The solid was collected by filtration and dried. [Yield: 9.45 g, 50% yield].

[References]

[1] Organic Process Research and Development, 2006, vol. 10, # 2, p. 285 - 288
[2] Patent: WO2007/125542, 2007, A2. Location in patent: Page/Page column 16
[3] Journal of Medicinal Chemistry, 1995, vol. 38, # 26, p. 4993 - 5006
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