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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-imidazole-2-carbaldehydeHCID 24955—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantN-(t-butoxycarbonyl)-N-(2-pyridinylmethyl)-N'-(5,6,7,8-tetrahydro-8-quinolinyl)-1,4-benzenedimethanamineHCID 22018600—
SolventMethanolHCID 887—
ProductHCID 9936460HCID 993646028.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183273B2
Source datasetuspto-grants-2007_02
ORD IDord-a2f5f9e0338c4750bec83241f00059ba
Source noteuspto-grants-2007_02