HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isoquinoline-1-carbaldehyde → HCID 58778825, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isoquinoline-1-carbaldehyde | HCID 265306 | — |
| Reactant | Iodo benzene diacetate | HCID 12217721 | — |
| Reactant | Methyl 2-(4-amino-3-hydroxyphenyl)acetate | HCID 17858854 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58778825 | HCID 58778825 | 33% |
Reaction Steps
In ethanol (5 ml), 1-isoquinolinecarbaldehyde (252 mg, 1.60 mmol) and methyl 4-amino-3-hydroxyphenylacetate (349 mg, 1.93 mmol) were stirred at room temperature for 12 hours. Iodobenzene diacetate (619 mg, 1.92 mmol) was added and the reaction mixture was stirred further at room temperature for 15 minutes. The reaction mixture was distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from n-hexane/ethyl acetate (4:1 to 3:1, v/v) eluate fractions, methyl (2-(1-isoquinolinyl)-6-benzoxazolyl)acetate (166 mg, 33%) was obtained as a yellow amorphous substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157487B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-1daef034f05b4546a407200a7bb54018 |
| Source note | uspto-grants-2007_01 |