2-Methyl-6-quinolinecarboxylic acid CAS 635-80-3
2-Methyl-6-quinolinecarboxylic acid Basic information
| Product Name: | 2-Methyl-6-quinolinecarboxylic acid |
| Synonyms: | 2-Methylquinoline-6-carboxylic acid 99%;2-METHYL-6-QUINOLINECARBOXYLIC ACID;2-METHYLQUINOLINE-6-CARBOXYLIC ACID;Quinaldine-6-carboxylic acid;2-Methyl-6-quinolinecarboxylic acid ,97%;6-Quinolinecarboxylicacid, 2-Methyl-;6-Carboxy-2-methylquinoline, 6-Carboxy-2-methyl-1-azanaphthalene;2-Methylquinoline-6-carboxylic Acid > |
| CAS: | 635-80-3 |
| MF: | C11H9NO2 |
| MW: | 187.19 |
| EINECS: | 251-785-3 |
| Product Categories: | Carboxylic Acids;Quinolines, Isoquinolines & Quinoxalines;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Carboxylic Acids;Quinolines, Isoquinolines & Quinoxalines;quinoline;Heterocyclic Compounds;Quinolines |
| Mol File: | 635-80-3.mol |
2-Methyl-6-quinolinecarboxylic acid Chemical Properties
| Melting point | 250 °C |
| Boiling point | 347.6±27.0 °C(Predicted) |
| density | 1.285±0.06 g/cm3(Predicted) |
| storage temp. | Sealed in dry,Room Temperature |
| form | Solid |
| pka | 3.13±0.30(Predicted) |
| color | White to Light yellow to Light orange |
| InChI | InChI=1S/C11H9NO2/c1-7-2-3-8-6-9(11(13)14)4-5-10(8)12-7/h2-6H,1H3,(H,13,14) |
| InChIKey | IZONZQFTYGVOOO-UHFFFAOYSA-N |
| SMILES | N1C2C(=CC(C(O)=O)=CC=2)C=CC=1C |
| CAS DataBase Reference | 635-80-3(CAS DataBase Reference) |
Safety Information
| Hazard Codes | Xn |
| Risk Statements | 22-36/37/38 |
| Safety Statements | 22-26-36/37/39 |
| Hazard Note | Irritant |
| HS Code | 29334900 |
| Chemical Properties | White solid |
| Uses | 2-Methylquinoline-6-carboxylic Acid is a preparation of arylpyrazolopyridine derivative as monoacylglycerol lipase modulators. |
| Synthesis | 150-13-0 123-73-9 635-80-3 General procedure for the synthesis of 2-methyl-6-quinoline carboxylic acid from p-aminobenzoic acid and trans-2-butenal:Intermediate 13: Synthesis of (2-methylquinolin-6-yl)methylamine:Step 1: Preparation of 2-methylquinoline-6-carboxylic acid: 6N hydrochloric acid (73 ml) was added to 4-aminobenzoic acid (5 g, 36.45 mmol) and heated to reflux for 2 hours. Subsequently, crotonaldehyde (3.06 g, 43.75 mmol) was added slowly and dropwise over 45 min. After 12 hours of reaction, the reaction mixture was cooled to 0 °C and the pH was adjusted to 3-5 with aqueous ammonia solution. the aqueous phase was extracted with dichloromethane, the organic phases were combined and acidified with 2N hydrochloric acid, the precipitate was collected by filtration and dried under vacuum to afford 2-methyl-6-quinolinecarboxylic acid as a brown solid (3.0 g, 44% yield). |
| References | [1] Patent: WO2013/144737, 2013, A2. Location in patent: Paragraph 252 [2] Patent: US2015/57309, 2015, A1. Location in patent: Paragraph 0524 [3] Journal of Medicinal Chemistry, 2002, vol. 45, # 21, p. 4647 - 4654 [4] Chemistry - A European Journal, 2018, vol. 24, # 61, p. 16368 - 16378 [5] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 22, p. 6138 - 6141 |
2-Methyl-6-quinolinecarboxylic acid Preparation Products And Raw materials
| Raw materials | Hydrochloric acid-->Dichloromethane-->PETROLEUM ETHER-->Sodium iodide-->4-Aminobenzoic acid-->Crotonaldehyde (trans predominantly)-->Paraldehyde |
