HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632576Generated: October 24, 2026
Sodium Bicarbonate → 1-cyclopentyl N-{3-[(methylamino)methyl]benzyl}-L-leucinate
https://huagongshe.com/en/reaction/632576
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 3-(Bromomethyl)benzaldehyde | HCID 7127825 | — |
| Reactant | L-leucine cyclopentyl ester tosylate | HCID 86633653 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-cyclopentyl N-{3-[(methylamino)methyl]benzyl}-L-leucinate | HCID 86686426 | 15.2% |
Reaction Steps
To a solution of 3-(bromomethyl)-benzaldehyde (0.513 g, 2.57 mmol) in dichloroethane (10 mL) was added L-leucine cyclopentyl ester tosylate (1.29 g, 3.46 mmol) and sodium triacetoxyborohydride (1.37 g, 6.46 mmol). The mixture was stirred for 30 minutes at room temperature then poured into ethyl acetate (200 mL). The organic extracts were washed with saturated ammonium chloride (2 times 50 mL) and water (50 mL). The organic extracts were then dried (MgSO4) and concentrated. The residue was dissolved in ethanol (30 mL) and methylamine hydrochloride (4.17 g, 61.7 mmol) was added followed by sodium hydrogen carbonate (4.32 g, 51 mmol). The mixture was stirred at room temperature for 18 hours then concentrated under vacuum, loaded directly onto a silica gel column and eluted with 95:5 dichloromethane:methanol to yield the desired product (0.130 g, 15% yield). LC/MS: m/z 333.25 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321718B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-91e262448bd24c2a981e1bc01796de64 |
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| Source note | uspto-grants-2016_04 |
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