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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121173Generated: November 1, 2026

Isoamyl Alcohol → HCID 54401291, compound

https://huagongshe.com/reaction/2121173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl AlcoholHCID 31260—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 10599017HCID 10599017—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54401291HCID 5440129138.7%

Reaction Steps

[4-(3-pyridylmethylamino)-2-phenylbenzoyl]methionine (200 mg, 0.46 mmol), prepared as in Example 192, carbonyldiimidazole (74 mg, 0.46 mmol), and isoamyl alcohol (40 mg, 0.46 mmol) were combined in 10 mL THF. After 2 hours at room temperature, sodium ethoxide (2.68 M in ethanol, 0.02 mmol) was added. After an additional 18 hours, the mixture was evaporated to dryness, partitioned between ethyl acetate and water, washed with water and brine, dried over Na2SO4, and chromatographed (Ethyl acetate) to give [4-(3-pyridylmethylamino)-2-phenylbenzoyl-L-methionine isoamyl ester (90 mg). MS m/e 506 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ 0.90 (d, J=7 Hz, 6H), 1.48 (m, 2H), 1.64 (m, 4H), 1.88 (m, 1H), 2.01 (s, 3H), 2.11 (t, J=7 Hz, 2H), 4.08 (m, 2H), 4.42 (s, 2H), 4.60 (m, 1H), 5.87 (d, J=8 Hz, 1H), 6.51 (d, J=3 Hz, 1H), 6.63 (m, 1H), 7.28-7.44 (m, 5H), 7.68 (m, 2H), 8.55 (m, 1H), 8.63 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06693123B2
Source datasetuspto-grants-2004_02
ORD IDord-0203567931ef42abb293ea936906d84b
Source noteuspto-grants-2004_02