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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278005Generated: October 27, 2026

(Naphthalen-2-yl)boronic acid → 5-(Naphth-2-yl)-3-(1-Methylpiperidin-4-yl)-4-Aza-1H-Indole

https://huagongshe.com/reaction/278005

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Naphthalen-2-yl)boronic acidHCID 2734375—
Reactant5-Trifluoromethanesulfonyloxy-3-(1-methylpiperidin-4-yl)pyrrolo[3,2-b]pyridineHCID 12041812—
Product5-(Naphth-2-yl)-3-(1-Methylpiperidin-4-yl)-4-Aza-1H-IndoleHCID 992796591.8%

Reaction Steps

O-Trifluoromethanesulfonyl-3-(1-methylpiperidin-4-yl)-5-hydroxy-4-aza-1H-indole (164 mg, 0.450 mmol) and 2-naphthylboronic acid (124 mg, 0.720 mmol) were converted to 141 mg of the title compound by the procedure of Example 3. (91%). MS(FD) m/e 341.8 (M+). EA calculated for C23H23N3: C, 80.94; H, 6.74; N, 12.32. Found: C, 88.11; H, 6.87; N, 12.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358972B1
Source datasetuspto-grants-2002_03
ORD IDord-9ac361d242d04deba14e57bacb2f6bbb
Source noteuspto-grants-2002_03