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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716767Generated: November 1, 2026

3-(1H-Indol-7-yl)-N-methyl-3-phenyl-propionamide → 3-(3-Methoxy-1H-indazol-6-yl)-N-methyl-3-pyridin-2yl-propionamide

https://huagongshe.com/reaction/1716767

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1H-Indol-7-yl)-N-methyl-3-phenyl-propionamideHCID 59831745—
ReactantHCID 67355209HCID 67355209—
Product3-(3-Methoxy-1H-indazol-6-yl)-N-methyl-3-pyridin-2yl-propionamideHCID 59831718—

Reaction Steps

3-(3-Methoxy-1H-indazol-6-yl)-N-methyl-3-pyridin-2yl-propionamide CCXLVI was prepared from 3-(3-methoxy-1H-indazol-6-yl)-N-methyl-3-pyridin-2yl-acrylamide using the procedure described for preparation of 3-(1H-Indol-7-yl)-N-methyl-3-phenyl-propionamide XIX (Example 4). The crude product (90% yield) was purified via chiral preparative HPLC by multiple injections onto 20×250 mm Chiralpak AD preparative column using a mixture of 60/40 hexane/isopropanol at 7 ml/min affording the enantiomer CCXLVI-A (αD=−0.269°) and the enantiomer CCXLVI-B (αD=+0.209°).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803830B2
Source datasetuspto-grants-2010_09
ORD IDord-e9b2dc76abb547ebadd1f7ad65947083
Source noteuspto-grants-2010_09