Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984811Generated: November 3, 2026

Pyridine → HCID 68870800, compound

https://huagongshe.com/reaction/1984811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3,5,5-Trimethylhexanoyl chlorideHCID 161929—
ReactantHCID 68870114HCID 68870114—
SolventDichloromethaneHCID 6344—
ProductHCID 58717686HCID 58717686—
ProductHCID 68870800HCID 68870800198.4%

Reaction Steps

A solution of (2S)-(2-amino-5-bromo-benzoylamino)-3-(2′-phenoxy-biphenyl-4-yl)-propionic acid methyl ester (54.5 mg, 0.10 mmol) from example 294 in 1 mL dry CH2Cl2 was treated with 3,5,5-trimethylhexanoyl chloride (1.2 eq., 23 μL, 0.12 mmol) and pyridine (1.5 eq., 12 μL, 0.15 mmol) in succession and stirred under an atmosphere of dry N2 for one hour, then concentrated in vacuo. The crude residue was purified by flash column chromatography (hexanes, EtOAc) to afford the desired amide, (2S)-[5-bromo-2-(3,3,5-trimethyl-hexanoylamino)-benzoylamino]-3-(2′-phenoxy-biphenyl-4-yl)-propionic acid methyl ester (68 mg). The methyl ester (20 mg, 29 μmol) was dissolved in 2.0 mL THF and 0.5 mL MeOH and saponified with 2N aqueous LiOH solution (0.25 mL), as described in general procedure C, to afford the title compound, (2S)-[5-bromo-2-(3,3,5-trimethyl-hexanoylamino)-benzoylamino]-3-(2′-phenoxy-biphenyl-4-yl)-propionic acid (20 mg), as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544699B2
Source datasetuspto-grants-2009_06
ORD IDord-6293918b6ad04656b0be0fee4349a9fe
Source noteuspto-grants-2009_06