HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448079Generated: October 29, 2026
1,3-Benzodioxole-5-carbonyl chloride → HCID 69188439, compound
https://huagongshe.com/reaction/448079
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Benzodioxole-5-carbonyl chloride | HCID 2734749 | — |
| Reactant | 3-Butyl-2,4,5-trimethylthiazol-3-ium iodide | HCID 69165591 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Product | HCID 69188439 | HCID 69188439 | — |
Reaction Steps
In a 20 mL vial 3-butyl-2,4,5-trimethylthiazol-3-ium iodide (48 mg in 0.5 mL DMA, 0.16 mmol, 1 equiv.) was added, followed by TEA (38 mg in 0.5 mL DMA, 0.37 mmol, 2.4 equiv.) and the solution went black. DMAP (2 mg in 0.5 mL DMA, 0.016 mmol, 0.1 equiv) was added next, followed by benzo[d][1,3]dioxole-5-carbonyl chloride (0.9 mL of 0.2M in DMA, 1.2 equiv). The mixture was shaken overnight at room temperature and then concentrated in vacuo. The resulting residue was taken up in 1:1 DMSO/MeOH and purified by reverse phase HPLC using a method analogous to that described in Example 53 to provide the title compound. 1H NMR (500 MHz, DMSO-d6/D2O) δ ppm 0.93 (t, 3 H) 1.34-1.44 (m, 2 H) 1.58-1.68 (m, 2 H) 2.16 (s, 3 H) 2.20 (s, 3 H) 4.02-4.09 (m, 2 H) 6.08 (s, 2 H) 6.48 (s, 1 H) 6.93-6.99 (m, 1 H) 7.47-7.48 (m, 1 H) 7.49-7.54 (m, 1 H); MS (ESI) m/z 332 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481574B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-61c5626b2ffe40b7b7185ba48e169ead |
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| Source note | uspto-grants-2013_07 |
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