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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250901Generated: November 1, 2026

Benzyl Bromide → Methyl 3-[2-benzyloxy-3'-(3-heptyl-1-methylureido)biphenyl-4-yl]propanoate

https://huagongshe.com/reaction/250901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3-[3'-(3-heptyl-1-methylureido)-2-hydroxybiphenyl-4-yl]propanoateHCID 11582687—
SolventMethyl Ethyl KetoneHCID 6569—
ProductMethyl 3-[2-benzyloxy-3'-(3-heptyl-1-methylureido)biphenyl-4-yl]propanoateHCID 67272651—

Reaction Steps

In a manner similar to that of Example (25a), by reaction of 300 μL (2.5 mmol, 2.7 eq) of benzyl bromide and 400 mg (0.93 mmol, 1 eq) of methyl 3-[3′-(3-heptyl-1-methylureido)-2-hydroxybiphenyl-4-yl]propanoate (prepared in Example 15f) in 10 ml of methyl ethyl ketone in the presence of 500 mg (3.61 mmol, 3.9 eq) of potassium carbonate at 90° C. for 3 hours, methyl 3-[2-benzyloxy-3′-(3-heptyl-1-methylureido)biphenyl-4-yl]propanoate is obtained in oil form and is used in the following reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863332B2
Source datasetuspto-grants-2011_01
ORD IDord-42ded9a6d9bb4a3196985bb2983f42c8
Source noteuspto-grants-2011_01