HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716509Generated: October 31, 2026
Thionyl Chloride → 2-Bromoimidazo[2,1-b]thiazole-6-carbonyl azide
https://huagongshe.com/reaction/716509
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | 2-Bromoimidazo[2,1-b]thiazole-6-carboxylic acid | HCID 12744615 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromoimidazo[2,1-b]thiazole-6-carbonyl azide | HCID 58310235 | 80% |
Reaction Steps
Thionyl chloride (0.33 mol) was added to 2-bromoimidazo[2,1-b]thiazole-6-carboxylic acid (13.1 mmol). The reaction mixture was stirred at 85° C. during 3 hrs. The mixture was then concentrated under vacuum and the residue was taken in acetone (40 mL). The sodium azide (14.4 mmol) in water (5.2 mL) was added in one portion at 0° C. and the mixture was stirred at 0-10° C. for 45 min. Water was added, and the solid filtered off and washed with water and then with a mixture of water/acetone (50/50). The solid was dried in vacuo to give compound 9 as a beige solid in 80% yield. 1H NMR (DMSO-d6, 400 MHz) δ (ppm) 8.27 (s, 1H), 8.49 (s, 1H); and MS (ESI, EI+) m/z=272.05-274.07 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187496B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-8b634c5bef6842e691d610e4791aa1ed |
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| Source note | uspto-grants-2015_11 |
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