HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84645Generated: October 29, 2026
Thionyl Chloride → HCID 86634856, compound
https://huagongshe.com/reaction/84645
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(4-(2-chlorophenyl)-1-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-8-carboxylic acid | HCID 86634857 | — |
| Product | HCID 86634856 | HCID 86634856 | — |
Reaction Steps
A solution of 2-(4-(2-chlorophenyl)-1-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-8-carboxylic acid (300 mg, 0.66 mmol) in 10 mL of SOCl2 was heated at 80° C. for 3 h. Concentration gave the crude acid chloride, 2-(4-(2-chlorophenyl)-1-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-8-carbonyl chloride which was slowly added (ca. 312 mg, ca. 0.66 mmol in 10 mL of THF), to a solution of NH3 (saturated solution in THF) and pyridine (0.5 mL) in 5 mL of THF at 0° C. The mixture was stirred at room temperature overnight, Diluted with water, the solids were washed with water and dried in vacuum. The crude product was purified by HPLC separation, gave 160.1 mg of 363, isolated yield: 54%. ESI-MS: 453. 1H NMR (DMSO-d6, 400 MHz): δ 7.98-7.41 (m, 9H, ArH, NH2), 6.49 (s, 1H, ═CH), 4.20 (s, 2H, CH2), 3.49 (s, 3H, CH3), 2.99 (s, 2H, CH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846762B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-32a70e9b25864b0dbb78fd252773da00 |
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| Source note | uspto-grants-2014_09 |
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