HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894120Generated: October 31, 2026
HCID 178434627, compound → HCID 178434626, compound
https://huagongshe.com/reaction/894120
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178434627 | HCID 178434627 | — |
| Reactant | HCID 178470423 | HCID 178470423 | — |
| Product | HCID 178434626 | HCID 178434626 | — |
| Product | HCID 178470423 | HCID 178470423 | — |
Reaction Steps
In a method for synthesizing 7-alkylamino-3-methylpyrazolo[4,3-d]pyrimidines, including the steps of esterifying 3-methyl-4-nitropyrazole-5-carboxylic acid to ethyl 3-methyl-4-nitropyrazole-5-carboxylate, forming 3-methyl-4-nitropyrazole-5-carboxamide from ethyl 3-methyl-4-nitropyrazole-5-carboxylate, catalytically reducing and formylating ethyl 3-methyl-4-nitropyrazole-5-carboxamide to produce 4-formylamino-3-methylpyrazole-5-carboxamide, closing the ring of 4-formylamino-3-methylpyrazole-5-carboxamide to produce 3-methyl-7-hydroxypyrazolo[4,3-d]pyrimidine, chlorinating said 3-methyl-7-hydroxypyrazolo [4,3-d]pyrimidine to produce 7-chloro-3-methylpyrazolo-[4,3-d], and reacting said 7-chloro-3-methylpyrazolo[4,3-d]pyrimidine with an alkylamine to produce a 7-alkylamino-3-methylpyrazolo[4,3-d]pyrimidine:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04282361 |
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| Source dataset | uspto-grants-1981_08 |
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| ORD ID | ord-b815209ddc444b1691310bfda21e1f33 |
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| Source note | uspto-grants-1981_08 |
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