HuagongsheHuagongshe Chemistry Print Report · For research reference only
(2-Methoxyethyl)(methyl)amine → HCID 59199293, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (2-Methoxyethyl)(methyl)amine | HCID 300977 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 59199232 | HCID 59199232 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 59199293 | HCID 59199293 | — |
Reaction Steps
To the solution of 4-(8-formylquinazolin-2-ylamino)benzenesulfonamide (11 mg, 30 umole) and 2-methoxy-N-methylethanamine (37 ul, 30 umole) in 500 ul of NMP was added a few drops of acetic acid. The reaction solution was stirred at room temperature for overnight. Sodium triacetoxy borohydride (7 mg, 33 umole) was added. The reaction mixture was stirred for 2 hr at ambient temperature. The reductive amination went to completion to give 4-(8-(((2-methoxyethyl)(methyl)amino)methyl)quinazolin-2-ylamino)benzenesulfonamide that was then purified on prep HPLC to give product as powder. ES/MS m/z 402.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932262B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-67cb58c2d1d742abae92280998e83f2d |
| Source note | uspto-grants-2011_04 |