HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309632Generated: November 1, 2026
Methyl Isobutyl Ketone → HCID 20185173, compound
https://huagongshe.com/reaction/2309632
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-(2-Thienyl)ethyl methanesulphonate | HCID 3047723 | — |
| Reactant | HCID 20037917 | HCID 20037917 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20185173 | HCID 20185173 | 76% |
Reaction Steps
A mixture of 7.9 parts of 3-[(4-fluorophenylmethyl)-2-(4-piperidinylmethyl)-3H-imidazo[4,5-b]pyridine dihydrochloride, 8.5 parts of sodium carbonate and 120 parts of 4-methyl-2-pentanone was stirred and refluxed for 30 minutes using a water separator. 7.8 Parts of 2-thiopheneethanol methanesulfonate (ester) were added and the whole was stirred and refluxed for 4 hours using a water separator. After cooling, the salts were filtered off, washed with 4-methyl-2-pentanone and the filtrate was washed with water. The organic layer was dried, filtered and evaporated. The residue was converted into the hydrochloride salt in 2-propanol and 2-propanone. The salt was filtered off and dried in vacuo at 60° C., yielding 8.0 parts (76%) of 3-[(4-fluorophenyl)methyl]-2-[[1-[2-(2-thienyl)ethyl]-4-piperidinyl]methyl]-3H-imidazo[4,5-b]pyridine dihydrochloride. monohydrate; mp. 210.8° C. (117).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04695575 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-6c078029ea124d4387786bbd6a8f70ed |
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| Source note | uspto-grants-1987_09 |
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