HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → N-Methyl-5-(1-methyl-1H-imidazol-2-yl)-N-propyl-isophthalamic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-Methyl-5-(1-methyl-1H-imidazol-2-yl)-N-propyl-isophthalamic acid methyl ester | HCID 68814383 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-Methyl-5-(1-methyl-1H-imidazol-2-yl)-N-propyl-isophthalamic acid | HCID 68814352 | — |
Reaction Steps
Dissolve N-methyl-5-(1-methyl-1H-imidazol-2-yl)-N-propyl-isophthalamic acid methyl ester (100 mg, 0.32 mmol) in methanol (10 mL). Dropwise add 1 N lithium hydroxide (0.38 mL) and stir overnight at room temperature. Add 2 N NaOH (0.1 mL) and stir for 48 h at room temperature. Acidify the mixture to about pH=6 by DOWEX® 50WX2-100 ion exchange resin and filter. Concentrate filtrate and lyophilize (1:1 acetonitrile:water) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07585885B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-b7b28d4dfa814e40a5acd32a0cd00711 |
| Source note | uspto-grants-2009_09 |