HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047640Generated: October 30, 2026
N'-Hydroxybenzenecarboximidamide → HCID 67300490, compound
https://huagongshe.com/reaction/2047640
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N'-Hydroxybenzenecarboximidamide | HCID 69186 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 2-oxopiperidine-4-carboxylate | HCID 23093678 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67300490 | HCID 67300490 | 53.6% |
Reaction Steps
Add benzamidoxime (5.63 g, 41.36 mmol) to a 1M solution of potassium t-butoxide (31 mL, 31 mmol) in tetrahydrofuran and anhydrous tetrahydrofuran (442 mL). Add methyl 2-oxopiperidine-4-carboxylate (5 g, 31.8 mmol) and stir overnight at room temperature. Pour reaction over saturated aqueous sodium bicarbonate and extract into chloroform. Separate layers and extract the aqueous phase with additional chloroform. Dry the combined organic layers over anhydrous magnesium sulfate, filter, and concentrate to dryness under reduced pressure. Purify the resulting residue by flash chromatography (silica gel), eluting with 1-5% 7 N ammoniated methanol in dichloromethane to afford the title compound (4.15 g). 1H NMR (CDCl3) δ 2.19 (m, 1H), 2.34 (m, 1H), 2.8-2.95 (m, 2H), 3.44-3.52 (m, 2H), 3.57 (m, 1H), 6.13 (bs, 1H), 7.45-7.54 (m, 3H), 8.0-8.11 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592590B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-79b38f5ab4bb4213ba202d4f038bd7da |
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| Source note | uspto-grants-2013_11 |
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