HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220123Generated: October 28, 2026
3-Chloro-4-(2-pyridylmethoxy)aniline → 4-(3-Chloro-4-(pyridin-2-ylmethoxy)phenylamino)-quinazoline-6-carboxylic acid methoxymethylamide
https://huagongshe.com/reaction/220123
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-4-(2-pyridylmethoxy)aniline | HCID 16781212 | — |
| Reactant | 4-Chloroquinazoline-6-carboxylic acid methoxymethylamide | HCID 86630923 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(3-Chloro-4-(pyridin-2-ylmethoxy)phenylamino)-quinazoline-6-carboxylic acid methoxymethylamide | HCID 68753790 | 76.2% |
Reaction Steps
4-Chloroquinazoline-6-carboxylic acid methoxymethylamide (XIV-1, 5.78 g) was dissolved in tetrahydrofuran (100 ml), and 5.39 g of 3-chloro-4 (pyridin-2-ylmethoxy)aniline was added, followed by stirring at 60° C. for 1 hour. A precipitate was filtered, and washed with tetrahydrofuran to obtain 4-(3-chloro-4-(pyridin-2-ylmethoxy)phenylamino)-quinazoline-6-carboxylic acid methoxymethylamide (XI-2, 7.87 g) as a white solid. The filtrate was allowed to stand at room temperature, and the resulting precipitate was collected by filtration, to newly obtain 2.21 g of XI-2.
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-8ded8dd40a514f9387d69b4c64f5bd37 |
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| Source note | uspto-grants-2012_06 |
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