HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Iodobenzaldehyde → 2-Amino-5-(p-iodobenzyl)aminomethylpyrrolo[2,3-d]pyrimidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Iodobenzaldehyde | HCID 96657 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-Amino-5-aminomethylpyrrolo[2,3-d]pyrimidin-4-one | HCID 20246377 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Amino-5-(p-iodobenzyl)aminomethylpyrrolo[2,3-d]pyrimidin-4-one | HCID 20468571 | 61.6% |
Reaction Steps
In 40 ml of dry methanol were suspended 126 mg of 2-amino-5-aminomethylpyrrolo[2,3-d]pyrimidin-4-one (dihydrochloride) and 116 mg of p-iodobenzaldehyde. After addition of 1 N methanolic sodium methoxide, the mixture was stirred at room temperature for 30 min. To this mixture was added 76 mg of sodium borohydride and the reaction was conducted at room temperature for 15 min. The reaction was then terminated by addition of 500 mg silica gel. The solvent was distilled off under reduced pressure and the residue was purified by silica gel chromatography to give 121 mg of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04435570 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-c036a8432ed64ce7bb8e831aa6ac3d50 |
| Source note | uspto-grants-1984_03 |