2-AMINO-4,7-DIHYDRO-5H-THIENO[2,3-C]PYRIDINE-3,6-DICARBOXYLIC ACID 6-TERT BUTYL ESTER 3-ETHYL ESTER manufacturers
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| | 2-AMINO-4,7-DIHYDRO-5H-THIENO[2,3-C]PYRIDINE-3,6-DICARBOXYLIC ACID 6-TERT BUTYL ESTER 3-ETHYL ESTER Basic information |
| Product Name: | 2-AMINO-4,7-DIHYDRO-5H-THIENO[2,3-C]PYRIDINE-3,6-DICARBOXYLIC ACID 6-TERT BUTYL ESTER 3-ETHYL ESTER | | Synonyms: | Ethyl2-amino-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate,N-BOCprotected95%;Ethyl 2-amino-6-Boc-4,7-dihydro-5H-thieno[2,3-c]pyridine-3-carboxylate;6-O-tert-butyl 3-O-ethyl 2-amino-5,7-dihydro-4H-thieno[2,3-c]pyridine-3,6-dicarboxylate;2-AMINO-4,7-DIHYDRO-5H-THIENO[2,3-C]PYRIDINE-3,6-DICARBOXYLIC ACID 6-TERT BUTYL ESTER 3-ETHYL ESTER;6-TERT-BUTYL 3-ETHYL-2-AMINO-4,5-DIHYDRO-THIENO[2,3-C]PYRIDINE-3,6(7H)-DICARBOXYLATE;6-(TERT-BUTYL) 3-ETHYL 2-AMINO-4,7-DIHYDROTHIENO[2,3-C]PYRIDINE-3,6(5H)-DICARBOXYLATE;BUTTPARK 75\08-01;Ethyl 2-amino-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate, N-BOC protected | | CAS: | 193537-14-3 | | MF: | C15H22N2O4S | | MW: | 326.41 | | EINECS: | 251-156-6 | | Product Categories: | CHIRAL CHEMICALS;Esters;Fused Ring Systems | | Mol File: | 193537-14-3.mol | ![2-AMINO-4,7-DIHYDRO-5H-THIENO[2,3-C]PYRIDINE-3,6-DICARBOXYLIC ACID 6-TERT BUTYL ESTER 3-ETHYL ESTER Structure](CAS/GIF/193537-14-3.gif) |
| | 2-AMINO-4,7-DIHYDRO-5H-THIENO[2,3-C]PYRIDINE-3,6-DICARBOXYLIC ACID 6-TERT BUTYL ESTER 3-ETHYL ESTER Chemical Properties |
| Melting point | 153 °C | | Boiling point | 492.5±45.0 °C(Predicted) | | density | 1.252±0.06 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | pka | 0.40±0.20(Predicted) | | Appearance | Light yellow to yellow Solid | | CAS DataBase Reference | 193537-14-3(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36/39 | | Hazard Note | Irritant | | HS Code | 2934999090 |
| | 2-AMINO-4,7-DIHYDRO-5H-THIENO[2,3-C]PYRIDINE-3,6-DICARBOXYLIC ACID 6-TERT BUTYL ESTER 3-ETHYL ESTER Usage And Synthesis |
| Synthesis | General Steps:
Step a. Synthesis of 2-amino-4,7-dihydro-5H-thieno[2,3-c]pyridine-3,6-dicarboxylic acid 6-tert-butyl 3-ethyl ester
In anhydrous ethanol (50 mL), N-tert-butoxycarbonyl-4-piperidone (12.9 g), ethyl cyanoacetate (7.345 g), and sulfur powder (2.080 g) were mixed, followed by the addition of triethylamine (9 mL). The reaction mixture was stirred at room temperature for 16 hours. Upon completion of the reaction, the precipitate was collected by filtration and washed with ethanol to afford 2-amino-4,5-dihydrothieno[2,3-c]pyridine-3,6(7H)-dicarboxylic acid-6-tert-butyl ester (18.7 g, 88% yield).
Product characterization data:
1H NMR (300 MHz, CDCl3): δ 6.02 (s, 2H), 4.31 (s, 2H), 4.23 (q, 2H, J = 7.2 Hz), 3.58 (t, 2H, J = 6.0 Hz), 2.72-2.80 (br s, 2H), 1.44 (s, 9H), 1.30 (t, 3H, J = 7.2 Hz).
LC-MS (ESI) m/z: 327.0 (M + H)+. | | References | [1] Synlett, 2010, # 9, p. 1351 - 1354 [2] Patent: US2010/120805, 2010, A1. Location in patent: Page/Page column 44 [3] Journal of Medicinal Chemistry, 2010, vol. 53, # 20, p. 7316 - 7326 [4] Patent: WO2009/33581, 2009, A1. Location in patent: Page/Page column 62 [5] Journal of Medicinal Chemistry, 2012, vol. 55, # 7, p. 3101 - 3112 |
| | 2-AMINO-4,7-DIHYDRO-5H-THIENO[2,3-C]PYRIDINE-3,6-DICARBOXYLIC ACID 6-TERT BUTYL ESTER 3-ETHYL ESTER Preparation Products And Raw materials |
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