HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → [1-(5-carbamoyl-4-{[(2-chlorophenyl)propyl]oxy}-2-thienyl)-1H-imidazo[4,5-c]pyridin-6-yl]methyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3-{[1-(2-chlorophenyl)propyl]oxy}-5-[6-(hydroxymethyl)-1H-imidazo[4,5-c]pyridin-1-yl]thiophene-2-carboxamide | HCID 68766751 | — |
| Product | [1-(5-carbamoyl-4-{[(2-chlorophenyl)propyl]oxy}-2-thienyl)-1H-imidazo[4,5-c]pyridin-6-yl]methyl methanesulfonate | HCID 86647115 | — |
Reaction Steps
In a similar manner as described for example 49 (step 1), 1 g of 3-{[1-(2-chlorophenyl)propyl]oxy}-5-[6-(hydroxymethyl)-1H-imidazo[4,5-c]pyridin-1-yl]thiophene-2-carboxamide, 517 mg of methanesulfonyl chloride, and 457 mg of triethylamine in 19 ml dichloromethane give [1-(5-carbamoyl-4-{[(2-chlorophenyl)propyl]oxy}-2-thienyl)-1H-imidazo[4,5-c]pyridin-6-yl]methyl methanesulfonate as crude material that is used for step 2 without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273890B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-c8ab4544929547d9906703b34c96c1f1 |
| Source note | uspto-grants-2012_09 |