HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 1-(methylamino)isoquinoline-7-carboxylate → 1-(Methylamino)isoquinoline-7-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 1-(methylamino)isoquinoline-7-carboxylate | HCID 67491404 | — |
| Reactant | 2-Methoxy-7-quinolinecarboxylic acid | HCID 67491592 | — |
| Product | 1-(Methylamino)isoquinoline-7-carboxylic acid | HCID 67491472 | — |
Reaction Steps
The title compound was prepared by a method analogous to that described in Step 3 of Intermediate 19, using ethyl 1-(methylamino)isoquinoline-7-carboxylate. +ESI (M+H) 203.1; 1H NMR (400 MHz, DMSO-d6, δ): 13.03 (br. s., 1H), 8.87 (s, 1H), 8.06 (dd, J=8.51, 1.47 Hz, 1H), 7.97 (d, J=5.67 Hz, 1H), 7.85 (d, J=4.50 Hz, 1H), 7.75 (d, J=8.41 Hz, 1H), 6.91 (d, J=5.87 Hz, 1H), 2.95 (d, J=4.50 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08993586B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-7aa1c7370e8643c2befe6e53e512da2a |
| Source note | uspto-grants-2015_03 |