HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220118Generated: October 28, 2026
Water → 4-(3-Chloro-4 (3-fluorobenzyloxy)phenylamino)-quinazoline-6-carboxylic acid methoxy methyl amide
https://huagongshe.com/reaction/220118
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 4-(3-Chloro-4-(3-fluorobenzyloxy)phenylamino)-quinazoline-6-carboxylic acid methyl ester | HCID 46928115 | — |
| Product | 4-(3-Chloro-4 (3-fluorobenzyloxy)phenylamino)-quinazoline-6-carboxylic acid methoxy methyl amide | HCID 68748957 | — |
Reaction Steps
In tetrahydrofuran (230 ml) was dissolved 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino)-quinazoline-6-carboxylic acid methyl ester (X-1, 11.6 g), N,O-dimethylhydroxylamine hydrochloride (7.8 g) was added, and 2 mol/L iPrMgCl tetrahydrofuran solution (79.8 ml) was added dropwise over 30 minutes under ice cooling. After completion of addition, the mixture was stirred for 20 minutes under ice cooling and, after completion of the reaction, 200 ml of aqueous saturated ammonium chloride solution was added. After 100 ml of water was added to the mixture, the mixture was extracted with ethyl acetate, and the organic layer was dried over sodium sulfate. The filtrate was concentrated to obtain 4-(3-chloro-4 (3-fluorobenzyloxy)phenylamino)-quinazoline-6-carboxylic acid methoxy methyl amide (XI-1, 12.7 g) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202879B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-85876b108190431d9ad6ba5892fc912f |
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| Source note | uspto-grants-2012_06 |
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