HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176705Generated: October 30, 2026
Triethylamine → 6-{2-[2-(6-Methoxy-quinolin-4-yl)-4,5,6,7-tetrahydro-2H-indazol-5-ylamino]-acetyl}-4H-benzo[1,4]oxazin-3-one
https://huagongshe.com/reaction/1176705
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-(2-chloroacetyl)-3,4-dihydro-2H-1,4-benzoxazin-3-one | HCID 2764458 | — |
| Reactant | 2-(6-methoxy-quinolin-4-yl)-4,5,6,7-tetrahydro-2H-indazol-5-ylamine | HCID 59560603 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-{2-[2-(6-Methoxy-quinolin-4-yl)-4,5,6,7-tetrahydro-2H-indazol-5-ylamino]-acetyl}-4H-benzo[1,4]oxazin-3-one | HCID 11948459 | 10% |
Reaction Steps
To a solution of 2-(6-methoxy-quinolin-4-yl)-4,5,6,7-tetrahydro-2H-indazol-5-ylamine (50 mg, 0.2 mmol) in DMF (0.5 mL) was added 6-(2-chloro-acetyl)-4H-benzo[1,4]oxazin-3-one (0.05 g, 0.22 mmol) and Et3N (0.033 mL, 0.22 mmol). The reaction was heated to 50° C. and stirred for 12 h. The crude was purified directly by basic reverse phase HPLC to afford 0.8 mg (10%) of the title compound. HPLC: Rt=5.50 min. MS (ESI): exact mass calculated for C27H25N5O4, 483.19; m/z found, 484.5 [M+H]+. 1H NMR (500 MHz, CDCl3): 8.78 (d, J=4.7, 1H), 8.06 (d, J=9.1, 1H), 7.69-7.61 (m, 3H), 7.42 (d, J=2.6, 1H), 7.40 (dd, J=9.1, 2.6, 1H), 7.32 (d, J=4.7, 1H), 7.04 (d, J=8.9, 1H), 4.70 (s, 2H), 4.21 (s, 1H), 3.89 (s, 3H), 3.11-2.80 (m, 5H), 2.62-2.58 (m, 1H), 2.26-2.17 (m, 1H), 1.93-1.86 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842810B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-f049bf7dcf32420eb3fdc1cd1ba7eb7c |
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| Source note | uspto-grants-2010_11 |
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