HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460173Generated: November 4, 2026
Diisopropylethylamine → HCID 18771980, compound
https://huagongshe.com/reaction/460173
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl valinate hydrochloride | HCID 111190 | — |
| Reactant | 6-Bromopyridine-2-carbaldehyde | HCID 2757009 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18771980 | HCID 18771980 | — |
Reaction Steps
To a stirred solution of L-valine methyl ester hydrochloride (0.54 g, 3.24 mmol) in dry toluene (15 mL) at 80° C. was added DIEA (2.0 mL 11 mmol) followed by (6-bromo-2-pyridyl)formaldehyde (0.50 g, 2.70 mmol). The resulting mixture was heated at 80° C. for 3 h. The reaction was brought to RT and a solution of NaBH(OAc)3 (1.4 g, 6.75 mmol) in glacial AcOH (4 mL) was added. The resulting mixture was stirred for 15 h and concentrated by rotary evaporation. The resulting yellow oil was dissolved in CH2Cl2 (100 mL), washed with a saturated solution of NaHCO3 (aq) (50 mL), brine (50 mL), dried over Na2SO4, filtered, concentrated by rotary evaporation and purified by flash chromatography (2:1 hexanes/EtOAc) to afford the title compound as a pale-yellow oil. EI-MS m/z 301 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196104B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-04c53c17135440fba5536217cfc4e9a1 |
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| Source note | uspto-grants-2007_03 |
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