HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Ammonia methanol dichloromethane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 178480514 | HCID 178480514 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ammonia methanol dichloromethane | HCID 21584172 | — |
| Product | HCID 178475105 | HCID 178475105 | — |
Reaction Steps
To a solution of N-(2-{3-[(1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)-methyl]phenylsulfanyl}ethyl)guanidine.dihydrochloride (100 mg) in dry acetonitrile (1 mL) is added acetic anhydride (64 mg) et 4-dimethylaminopyridine (51 mg). After 24 hours at room temperature, solvent and volatiles are removed under reduced pressure. The residue is purified by chromatography (toluene/acetone/triethylamine 50/50/1 then gradient dichloromethane/methanol/ammonia from 95/5/0.5 to 90/10/1) to give N-acetyl-N′-(2-{3-[(1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)methyl]phenylsulfanyl}ethyl)guanidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08802664B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-c3ab9301ce3a4451b51814c208a8678b |
| Source note | uspto-grants-2014_08 |