HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14627Generated: October 30, 2026
HCID 22057577, compound → Ethyl 1-(aminomethyl)-6,8-dimethoxyisoquinoline-4-carboxylate
https://huagongshe.com/reaction/14627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22057577 | HCID 22057577 | — |
| Reactant | HCID 59341073 | HCID 59341073 | — |
| Product | Ethyl 1-(aminomethyl)-6,8-dimethoxyisoquinoline-4-carboxylate | HCID 11778955 | 123.5% |
Reaction Steps
To a solution of 1-(1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-6,8-dimethoxy-isoquinoline-4-carboxylic acid ethyl ester (1.22 g, 2.90 mmol) in 80 mL of absolute ethanol hydrazine monohydrate (1.59 g, 31.8 mmol) was added and the mixture was stirred under a nitrogen atmosphere at 40° C. After 4 h, the reaction was cooled to room temperature, and the phthalhydrazide precipitate was removed by filtration, rinsing with ethanol. The filtrate was concentrated under reduced pressure to give 1.04 g of crude 1-aminomethyl-6,8-dimethoxy-isoquinoline-4-carboxylic acid ethyl ester, which was used directly the next step. H1-NMR (DMSO): δ, 8.84 (s, 1H), 7.81 (d, 1, J=2.4 Hz), 6.76 (d, 1H, J=2.3 Hz), 4.36 (q, 2H, J=7.13), 4.32 (s, 2H), 3.95 and 3.88 (s, 3H each), 1.35 (t, 3H, J=7.2 Hz); MS: APCI (M+H) calc'd for C15H18N2O4+H 291.3; found 291.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07732446B1 |
|---|
| Source dataset | uspto-grants-2010_06 |
|---|
| ORD ID | ord-8c945fe9c735460ba4ece0143d86b834 |
|---|
| Source note | uspto-grants-2010_06 |
|---|