HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351162Generated: October 31, 2026
1H-imidazole-2-carbaldehyde → HCID 9936460, compound
https://huagongshe.com/reaction/351162
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1H-imidazole-2-carbaldehyde | HCID 24955 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | N-(t-butoxycarbonyl)-N-(2-pyridinylmethyl)-N'-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamine | HCID 22018600 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 9936460 | HCID 9936460 | 28.8% |
Reaction Steps
To a stirred solution of N-(tert-butoxycarbonyl)-N-(2-pyridinylmethyl)-N′-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamine (174 mg, 0.38 mmol) in dry MeOH (5 mL) was added 2-imidazolecarboxaldehyde (75 mg, 0.78 mmol) and sodium cyanoborohydride (55 mg, 0.88 mmol) and the mixture was stirred for 40 h. The reaction mixture was concentrated in vacuo and partitioned between CH2Cl2 (30 mL) and aqueous 1 N sodium hydroxide (30 mL). The aqueous layer was washed with CH2Cl2 (2×20 mL) and the combined organic extracts washed with brine (30 mL), dried (MgSO4), filtered and concentrated in vacuo. Purification of the crude product by column chromatography on silica gel (CH2Cl2/MeOH, 95:5) afforded the imidazole derivative (48 mg, 24%) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07183273B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-a2f5f9e0338c4750bec83241f00059ba |
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| Source note | uspto-grants-2007_02 |
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