HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(3-Methoxylphenyl)quinazoline-4-carboxylic acid → 2-[[2-(3-Methoxylphenyl)quinazolin-4-yl]carbonyl]-5-hydroxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(3-Methoxylphenyl)quinazoline-4-carboxylic acid | HCID 90410233 | — |
| Reactant | 6-Methoxy-1,2,3,4-tetrahydroisoquinolin-5-ol hydrochloride | HCID 90411180 | — |
| Product | 2-[[2-(3-Methoxylphenyl)quinazolin-4-yl]carbonyl]-5-hydroxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline | HCID 86269635 | 17% |
Reaction Steps
Reaction of 2-(3-methoxylphenyl)quinazoline-4-carboxylic acid with 5-hydroxy-6-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride gave compound 47 (17% yield) as a white solid. 1H NMR (300 MHz, DMSO-d6) δ 2.67 and 2.90 (2t, 2H), 3.50 and 4.04 (2t, 2H), 3.74-3.88 (4s, 6H), 4.39 and 4.92 (2s, 2H), 6.32 and 6.77 (2d, 1H), 6.70 and 6.91 (2d, 1H), 7.15-7.18 (m, 1H), 7.46-7.53 (m, 1H), 7.77-8.19 (m, 6H), 8.68-8.72 (2s, 1H); MS (ESI) m/z 442 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09193707B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-05b7d30b8f7a4b18b387a2d51023f06c |
| Source note | uspto-grants-2015_11 |