HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61666Generated: October 29, 2026
4-Chloro-7-methoxy-6-(2-methoxyethoxy)-2-(3-nitrophenyl)quinazoline → HCID 59361995, compound
https://huagongshe.com/reaction/61666
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chloro-7-methoxy-6-(2-methoxyethoxy)-2-(3-nitrophenyl)quinazoline | HCID 59361897 | — |
| Reactant | 5-amino-1H-indazole-1-carboxylate | HCID 86642411 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 59361995 | HCID 59361995 | 149.2% |
Reaction Steps
A mixture of 4-chloro-7-methoxy-6-(2-methoxyethoxy)-2-(3-nitrophenyl)quinazoline (0.500 g, 1.28 mmol) and 5-amino-1H-indazole-1-carboxylate (0.314 g, 1.34 mmol) in iso-propanol (30 mL) was heated at 95° C. for 30 minutes and at 95° C. for 8 h. The mixture was allowed to cool to RT and the solid was collected via filtration. The cake was washed with iso-propanol and Et2O, triturated with CH2Cl2 and EtOAc and dried in vacuo to give tert-Butyl 5-(7-methoxy-6-(2-methoxyethoxy)-2-(3-nitrophenyl)quinazolin-4-ylamino)-1H-indazole-1-carboxylate (0.560 g, 0.955 mmol, 71%). MS 587 (M+1). HPLC retention time 7.21 mins.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09440961B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-285c7538f9964a96a8c51fcc274aee98 |
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| Source note | uspto-grants-2016_09 |
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