HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 23130732, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-({[Ethoxy(hydroxy)methylidene]amino}methyl)isoleucine | HCID 124195 | — |
| Reactant | HCID 23130419 | HCID 23130419 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23130732 | HCID 23130732 | 54% |
Reaction Steps
To a solution of 6-amino-N-(5-(3-chloro-benzyl)-thiophen-2-ylmethyl)-nicotinamide described in Example A-145 (110 mg, 0.3 mmol) in methanol (10 mL) were added 5,5-dimethylimidazo phospho-2,4-dione (43 mg, 0.33 mmol) and an aqueous solution of 37% formaldehyde (0.5 mL), and the solution was stirred under reflux for 2 hours. NH silica gel was added to the reaction solution, the solvent was evaporated in vacuo for adsorption, purification was carried out by NH silica gel column chromatography (hexane:ethyl acetate=1:1, then ethyl acetate), and the title compound (65 mg, 0.16 mmol, 54%) was obtained as a slightly yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932272B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-e325a5fc3bdf4d5b8c04ee083e57e2a3 |
| Source note | uspto-grants-2011_04 |