HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161775Generated: October 29, 2026
Sodium cyanoborohydride → HCID 68648374, compound
https://huagongshe.com/reaction/1161775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 68648055 | HCID 68648055 | — |
| Reactant | HCID 68648217 | HCID 68648217 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68648374 | HCID 68648374 | — |
Reaction Steps
Add Preparation 10 (5.25 g) to a suspension of imidazolocyclohexy-3-amine hydrochloride (2 gm) (Preparation 8) in methanol (30 mL). Stir the mixture at room temperature for 30 min. Add sodium cyanoborohydride (1 g) and stir the mixture for 2 h. Heat the reaction mixture at 50° C. for 2 h. Dilute the reaction mixture with ethyl acetate (50 mL) and wash the mixture with water (50 mL). Dry ethyl acetate layer over sodium sulfate and concentrate on rotary evaporator to give a crude. Purify the crude by silica flash chromatography eluting with a gradient of 0-5% methanol in DCM to give the product as a mixture of diastereomers, 3-(4-benzyloxy-2,6-dichloro-benzyl)-1-(4,5,6,7-tetrahydro-3H-benzimidazole-3-yl)-pyrrolidin-2-one (4.5 gm). MS: m/z=470 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820659B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-b489c842f7d94d9fbe6a491006714aac |
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| Source note | uspto-grants-2010_10 |
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