HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584859Generated: November 1, 2026
Diethyl (ethoxymethylene)malonate → HCID 178469783, compound
https://huagongshe.com/reaction/1584859
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Product | HCID 178469783 | HCID 178469783 | 67% |
Reaction Steps
The title compound was prepared by (a) reaction of diethylethoxymethylenemalonate (6 g, 28 mmol) with acetamidine hydrochloride (3 g, 31 mmol) to afford 67% of ethyl 2-methyl-4-hydroxypyrimidine-5-carboxylate in analogy to Example 15, (b) reaction of ethyl 2-methyl-4-hydroxypyrimidine-5-carboxylate (2.8 g, 15 mmol) with POCl3 (46 g, 300 mmol) to afford 28% of ethyl 4-chloro-2-methylpyrimidine-5-carboxylate, (c) reaction of ethyl 4-chloro-2-methylpyrimidine-5-carboxylate (0.25 g, 1.25 mmol) with hydrazine (0.2 g, 6.3 mmol) to afford 96% of 4-hydrazino-2-methylpyrimidine-5-carboxylate in analogy to Example 18, (d) reaction of 4-hydrazino-2-methylpyrimidine-5-carboxylate (0.24 g, 1.2 mmol) with citraconic anhydride (0.16 g, 1.44 mmol) to afford 70% (0.24 g) of the title compound (m.p. 98-99° C.) in analogy to Example 21.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05935966 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-f14967b3a94d41cf81ea89fbb3c11765 |
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| Source note | uspto-grants-1999_08 |
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