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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642572Generated: November 1, 2026

3-Benzyloxy-1-propanol → 3-(5-(3-(ethylsulfonyl)phenyl)-3-methyl-9H-pyrido[2,3-b]indol-8-yloxy)propan-1-ol

https://huagongshe.com/reaction/1642572

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Benzyloxy-1-propanolHCID 347971—
Reactant5-(3-(ethylsulfonyl)phenyl)-3-methyl-9H-pyrido[2,3-b]indol-8-olHCID 58880081—
CatalystHCID 178506449HCID 178506449—
Product3-(5-(3-(ethylsulfonyl)phenyl)-3-methyl-9H-pyrido[2,3-b]indol-8-yloxy)propan-1-olHCID 58880136—

Reaction Steps

The title compound was synthesized from Compound 157 and 3-(benzyloxy)propan-1-ol using an analogous procedure to that outlined in the preparation of Compound 210 followed by debenzylation using Pd/C—H2 .1H NMR (400 MHz, DMSO-d6) δ ppm 1.18 (t, J=7.33 Hz, 3 H) 2.01 (t, J=6.19 Hz, 2 H) 2.27 (s, 3 H) 3.41 (q, J=7.33 Hz, 2 H) 3.72 (q, J=5.98 Hz, 2 H) 4.30 (t, J=6.19 Hz, 2 H) 4.57 (t, J=5.18 Hz, 1 H) 7.06-7.17 (m, 2 H) 7.55 (s, 1 H) 7.85 (t, J=7.71 Hz, 1 H) 8.00 (br. s., 1 H) 7.98 (d, J=5.05 Hz, 2 H) 8.08 (s, 1 H) 8.28 (s, 1 H) 11.99 (s, 1 H); ESI-MS: m/z calc'd for C23H24N2O4S 424.15; found 425.3 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119655B2
Source datasetuspto-grants-2012_02
ORD IDord-aff3771c69b6485ebe21d654f9f7419a
Source noteuspto-grants-2012_02