HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199350Generated: October 31, 2026
Water → N-(3-chloro-4-fluoro-phenyl)-7-(2-methoxyethoxy)-6-nitro-quinazolin-4-amine
https://huagongshe.com/reaction/2199350
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 2-Methoxyethanol | HCID 8019 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(3-chloro-4-fluorophenyl)-7-fluoro-6-nitroquinazolin-4-amine | HCID 10640649 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N-(3-chloro-4-fluoro-phenyl)-7-(2-methoxyethoxy)-6-nitro-quinazolin-4-amine | HCID 18765556 | 100% |
Reaction Steps
2-methoxyethanol (152 mg, 2 mmol) was dissolved in 30 mL of dimethyl sulfoxide in an ice-water bath, followed by addition of 60% sodium hydride (80 mg, 2 mmol). The mixture was warmed up to 40° C. and stirred for 2 hours, then N-(3-chloro-4-fluoro-phenyl)-7-fluoro-6-nitro-quinazolin-4-amine 8a (336 mg, 1 mmol) was added. The reaction mixture was stirred for 4 hours at 40° C., then warmed up to 50° C. and stirred for 12 hours. The reaction mixture was added with water (20 mL), filtered and the filter cake was washed with water (50 mL), dried under vacuum to obtain the title compound N-(3-chloro-4-fluoro-phenyl)-7-(2-methoxyethoxy)-6-nitro-quinazolin-4-amine 8b (392 mg, yield 100%) as a yellow solid, which was directly used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09358227B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-cfc3daeb8e3f4038af0018f2f02d2d4f |
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| Source note | uspto-grants-2016_06 |
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