HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848002Generated: October 30, 2026
Formaldehyde → 6-(Imidazo[1,2-a]pyridin-3-ylmethyl)-2-(methylthio)benzo[d]thiazole
https://huagongshe.com/reaction/1848002
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | 6-Ethynyl-2-(methylsulfanyl)-1,3-benzothiazole | HCID 86681026 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Catalyst | copper(II) trifluoromethanesulfonate | HCID 2734996 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-(Imidazo[1,2-a]pyridin-3-ylmethyl)-2-(methylthio)benzo[d]thiazole | HCID 86681027 | 38% |
Reaction Steps
A stirred mixture of 2-aminopyridine (100 mg, 1.1 mmol), paraformaldehyde (34 mg, 1.1 mmol), CuCl (5 mg, 0.06 mmol), and Cu(OTf)2 (19 mg, 0.06 mmol) in 3 mL of toluene in a pressure tube was flushed with argon. 6-Ethynyl-2-(methylthio)benzo[d]thiazole (327 mg, 1.6 mmol) from Step 3 of this Example was added. The reaction vessel was sealed and the mixture was heated in an oil bath at 120° C. for 6 h. LCMS analysis showed that the reaction was mostly complete. The reaction mixture was partitioned between EtOAc and saturated aq NaHCO3. The organic layer was washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The residue was purified by silica gel chromatography eluting with 0-100% EtOAc in hexanes to afford 6-(imidazo[1,2-a]pyridin-3-ylmethyl)-2-(methylthio)benzo[d]thiazole (127 mg, 38%) as a brown oil. LCMS (ESI) m/z 312 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952058B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-36ffaa4090384c57935bbcd0a0b18781 |
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| Source note | uspto-grants-2015_02 |
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