HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858208Generated: November 2, 2026
p-Aminophenylacetic acid ethyl ester → HCID 22125060, compound
https://huagongshe.com/reaction/1858208
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Aminophenylacetic acid ethyl ester | HCID 225219 | — |
| Reactant | 3-(2,6-dichlorophenyl)-7-methanesulfonyl-1-methyl-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-one | HCID 18425444 | — |
| Product | HCID 22125060 | HCID 22125060 | 38% |
Reaction Steps
A mixture of 200 mg (0.52 mmol) of 3-(2,6-dichlorophenyl)-3,4-dihydro-7-methanesulfonyl-1-methylpyrimido[4,5-d]pyrimidin-2(1H)-one and 800 mg (4.47 mmol) of ethyl 4-aminophenylacetate was heated at 185° C. for 45 minutes. The residue was partitioned between 10 ml of ethyl acetate and 10 ml of 2M hydrochloric acid and the insoluble cream colored solid was collected by filtration and washed with 20 ml of water and 20 ml of ethyl acetate and then dried under a high vacuum. 95 mg (38%) of ethyl 2-[4-[[3-(2,6-dichlorophenyl)-1,2,3,4-tetrahydro-1-methyl-2-oxopyrimido[4,5-d]pyrimidin-7-yl]amino]phenyl]acetate of melting point 211-212° C. were isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06150373 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-adb53c97ee8149069711ffc3c25fb204 |
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| Source note | uspto-grants-2000_11 |
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