HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Chloromethyl-1,4-dichloro-isoquinoline → 4-chloro-7-(hydroxymethyl)-1(2H)-isoquinolone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Chloromethyl-1,4-dichloro-isoquinoline | HCID 18698312 | — |
| Reactant | Ethyl 4-chloro-1-oxo-1,2-dihydro-7-isoquinolinecarboxylate | HCID 18698325 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-chloro-7-(hydroxymethyl)-1(2H)-isoquinolone | HCID 18698430 | 86% |
Reaction Steps
7-(Chloromethyl)-1,4-dichloro-isoquinoline ##STR186## LiBH4 (530 mg, 24.3 mmol) was added portionwise to a stirred solution of ethyl 4-chloro-1-oxo-1,2-dihydro-7-isoquinolinecarboxylate (3.06 g, 12.2 mmol) in THF (100 mL) and the mixture was stirred at room temperature for 1 h. The heterogeneous mixture was quenched with dilute HCl (2 M), and extracted with CH2Cl7 (2×100 mL) and EtOAc (5×100 mL). The remaining solid was taken up in hot EtOH, and allowed to cool to yield a white fluffy solid. This solid was combined with the combined organic extracts, evaporated in vacuo and crystallised with EtOH to give 4-chloro-7-(hydroxymethyl)-1(2H)-isoquinolone (2.19 g, 10.49 mmol) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093731 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-8f71c2a4eb4345d680effc9fd3c5fda7 |
| Source note | uspto-grants-2000_07 |