HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260550Generated: October 27, 2026
Ethyl Acetate → N-(4-(4-(6-isopropoxypyridazin-3-yloxy)phenyl)butan-2-yl)acetamide
https://huagongshe.com/reaction/1260550
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Chloro-6-isopropoxypyridazine | HCID 252823 | — |
| Reactant | N-[3-(4-Hydroxyphenyl)-1-methylpropyl]acetamide | HCID 59956161 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | N-(4-(4-(6-isopropoxypyridazin-3-yloxy)phenyl)butan-2-yl)acetamide | HCID 49858288 | — |
Reaction Steps
N-[3-(4-Hydroxyphenyl)-1-methylpropyl]acetamide (311 mg, 1.5 mmol) was dissolved in 3 ml of NMP, admixed with sodium hydride (55% in oil) (120 mg, 3 mmol) and, after addition of 3-chloro-6-isopropoxypyridazine (259 mg, 1.5 mmol) stirred in a microwave reactor at 150° C. for 15 min. Following addition of ethyl acetate and water, the organic phase was separated off, concentrated and purified by preparative HPLC (PR18, acetonitrile/water 0.1% TFA). Yield: 40mg (8%), M+H+: 344.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470841B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-29f8be87b45d4bdb9e589d83e2752d15 |
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| Source note | uspto-grants-2013_06 |
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