7-Chlorothieno[3,2-b]pyridine synthesis
- Product Name:7-Chlorothieno[3,2-b]pyridine
- CAS Number:69627-03-8
- Molecular formula:C7H4ClNS
- Molecular Weight:169.63
107818-20-2
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69627-03-8
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Yield:69627-03-8 96%
Reaction Conditions:
Stage #1: thieno[3,2-b]pyridin-7-olwith trichlorophosphate at 60 - 100; for 3.5 h;
Stage #2: with ammonia;water monomer at 0;
Steps:
1
7-Chlorothieno[3,2-6]pyridine (6); To neat POCl3 (200 mL, 2146 mmol) at 6O0C in a 500 mL round-bottom flask was added thieno[3,2-&]pyridin-7-ol (1 eq., 200 g, 1323 mmol) in small portions over 1.5 h. The reaction mixture was heated at 6O0C for Ih and at 1000C for an additional hour. After cooling down to O0C, the reaction mixture was poured onto crushed ice (1 L) over a period of 30 min. After 15 min, NH4OH (1.5 L) was added to the mixture to form a grey precipitate that was collected by filtration, washed with water (50 mL) and air dried. The dry solid was suspended in EtOAc (1 L). The slurry was stirred at r.t. for 15 min, filtered and the filter was washed with EA (2x 100 mL). The organic phase was collected, dried over MgSO4 and concentrated. The residue was passed through a short silica gel pad (300 g, eluent - a gradient hexane/EtOAc, 8/2 to 5/5) and dried in the vacuum oven (350C) for 2h to afford 6 as a off-white solid (214.8 g, 1266 mmol, 96% yield). MS (m/z): 170.0 (M+H). 1H NMR (400 MHz, DMSO-d6) δ (ppm): 8.64 (d, J = 5.1 Hz, IH), 8.25 (d, J = 5.5 Hz, IH), 7.66 (d, J = 5.5 Hz, IH), 7.54 (d, J = 5.1 Hz, IH).
References:
WO2009/26720,2009,A1 Location in patent:Page/Page column 93; 94
69627-02-7
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69627-03-8
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104273-29-2
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79-37-8
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69627-03-8
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