HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3216Generated: October 26, 2026
Acetic Acid → 2-aminopyrido[2,3-d]pyrimidin-7(8H)-one 55
https://huagongshe.com/reaction/3216
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl 3-aminobenzoate | HCID 11400 | — |
| Reactant | 6-(2,6-Dichlorophenyl)-8-methyl-2-methylsulfonyl-8H-pyrido[2,3-d]pyrimidin-7-one | HCID 10596157 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-aminopyrido[2,3-d]pyrimidin-7(8H)-one 55 | HCID 5327901 | — |
Reaction Steps
A mixture of 0.226 g (0.58 mmol) of 6-(2,6-dichlorophenyl)-2-methanesulfonyl-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 39 and 0.40 g (2.42 mmol) of 3-aminobenzoic acid, ethyl ester was fused in a 170° C. oil bath to give a clear melt. After 6 minutes, the melt was cooled to ca. 100° C. Glacial acetic acid (1 mL) was added to dissolve the melt. Water (5 mL) was added to precipitate a solid. The solid was filtered, washed well with water, and triturated with 2 mL of methanol. The mixture was filtered, and the cake was washed with 1 mL of methanol and then ether; wt 0.194 g. Recrystallization from ethyl acetate gave pure product; wt 0.075 g; mp 238°-240° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05733914 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-9fd5cd2b22e5454fb149f6f3ed738293 |
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| Source note | uspto-grants-1998_03 |
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