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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494048Generated: October 30, 2026

Phenylboronic Acid → HCID 86617218, compound

https://huagongshe.com/reaction/494048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylboronic AcidHCID 66827—
ReactantTolylboronic acidHCID 79799—
Reactant2-Methylphenyl boronic acidHCID 2733267—
Reactant3-Tolylboronic acidHCID 2733950—
ReactantHCID 86617221HCID 86617221—
ProductHCID 86617218HCID 86617218—
ProductHCID 86617219HCID 86617219—
ProductHCID 86617220HCID 86617220—

Reaction Steps

Proceeding as described in Example 6 above, but substituting tert-butyl 2-(4-((3-bromophenyl)(phenyl)methyl)piperazin-1-yl)acetate with 2-((R)-2-methyl-4-((R)-(4-bromophenyl)(phenyl)methyl)piperazin-1-yl)acetate and treating it with phenylboronic acid, 2-methylphenylboronic acid, 3-methylphenylboronic acid and 4-methylphenylboronic acid provided tert-butyl ((R)-2-methyl-4-((R)-(4-biphenyl)(phenyl)methyl)-piperazin-1-yl)acetate, tert-butyl ((R)-2-methyl-4-((R)-(4-(2-methylphenyl)phenyl)(phenyl)methyl)-piperazin-1-yl)acetate, tert butyl ((R)-2-methyl-4-((R)-(4-(3-methylphenyl)phenyl)-(phenyl)methyl)-piperazin-1-yl)acetate, and tert-butyl ((R)-2-methyl-4-((R)-(4-(4-methylphenyl)phenyl)-(phenyl)methyl)-piperazin-1-yl)acetate respectively, which were converted to [(R)-4-((R)-biphenyl-4-yl-phenyl-methyl)-2-methyl-piperazin-1-yl]-acetic acid; {(R)-2-methyl-4-[(R)-(2′-methyl-biphenyl-4-yl)-phenyl-methyl]-piperazin-1-yl}-acetic acid; {(R)-2-methyl-4-[(R)-(3′-methyl-biphenyl-4-yl)-phenyl-methyl]-piperazin-1-yl}-acetic acid; and {(R)-2-methyl-4-[(R)-(4′-methyl-biphenyl-4-yl)-phenyl-methyl]-piperazin-1-yl}-acetic acid, respectively, as described in Example 4 above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538114B2
Source datasetuspto-grants-2009_05
ORD IDord-2316d65eda244aa09cf1954ac8ea8b78
Source noteuspto-grants-2009_05