HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470767Generated: October 31, 2026
2-Methyltetrahydrofuran → N-((1S)-1-(4-(1-(4-((2-methylcyclopropyl)methoxy)phenyl)-piperidin-4-yl)phenyl)ethyl)acetamide
https://huagongshe.com/reaction/1470767
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | (2-Methylcyclopropyl)methanol | HCID 138655 | — |
| Reactant | (S)-N-{1-(4-[1-(4-Hydroxyphenyl)-piperidin-4-yl]-phenyl}-ethyl)-acetamide | HCID 67125424 | — |
| Product | N-((1S)-1-(4-(1-(4-((2-methylcyclopropyl)methoxy)phenyl)-piperidin-4-yl)phenyl)ethyl)acetamide | HCID 67970640 | — |
Reaction Steps
50 mg (0.15 mmol) (S)—N-{1-(4-[1-(4-Hydroxyphenyl)-piperidin-4-yl]-phenyl}-ethyl)-acetamide (compound 1.48), 14 mg (0.16 mmol) 2-methylcyclopropanemethanol and 38.8 mg (0.15 mmol) triphenylphosphine are added to 2 mL 2-methyl-tetrahydrofurane at 0° C. 30.5 μl (0.15 mmol) di-iso-propyl azodicarboxylate are added and the mixture is allowed to warm to rt. Stirring is continued over night followed by addition of 0.5 equivalents of triphenylphosphine and 0.5 equivalents of di-iso-propyl azodicarboxylate. Stirring is continued for one day and again additional triphenylphosphine and di-iso-propyl azodicarboxylate are added and stirring is continued for 16 h at 50° C. Then the mixture is filtered and purified using reversed phase HPLC (water/MeOH, 0.1% FA) to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006450B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-a9b1195a2a894575b84b9977b7961a82 |
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| Source note | uspto-grants-2015_04 |
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