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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295154Generated: October 31, 2026

(4-Methoxy-phenyl)-propynoic acid ethyl ester → 7-(2-{1-[2-Ethoxycarbonyl-1-(4-methoxy-phenyl)-vinyl]-1H-indol-5-yloxy}-ethyl)-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1295154

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Methoxy-phenyl)-propynoic acid ethyl esterHCID 12253119—
Reactant7-[2-(1H-indol-5-yloxy)-ethyl]-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl esterHCID 66821083—
Product7-(2-{1-[2-Ethoxycarbonyl-1-(4-methoxy-phenyl)-vinyl]-1H-indol-5-yloxy}-ethyl)-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl esterHCID 6682145188%

Reaction Steps

The title compound was synthesized from (4-methoxy-phenyl)-propynoic acid ethyl ester and 7-[2-(1H-Indol-5-yloxy)-ethyl]-3,4-dihydro-2H-[1,8]naphthyridine-1-carboxylic acid tert-butyl ester using the procedure described in Example 16, step (d1), in a 88% yield as an E/Z isomeric mixture. 1H NMR (CDCl3) [E/Z mixture] δ 7.32 (m, 2H), 7.21 (m, 1H), 7.11–6.85 (m, 6H), 6.70 (m, 1H), 6.50 (m, 111), 6.13 (s, 0.5H), 6.03 (s, 0.5H), 4.40 (m, 2H), 4.10 (q, 2H, J=7.2 Hz), 3.86 (s, 1.5H), 3.83 (s, 1H), 3.76(t, 2H, J=5.2 Hz), 3.70 (t, 2H, J=6.0 Hz), 3.20 (t, 2H, J=6.8 Hz), 2.70 (t, 2H, J=6.8 Hz, J=6.8 Hz), 1.90 (m, 2H), 1.49 (s, 9H), 1.23 (t, 1.5H, J=7.2 Hz), 1.18 (t, 1.5H, J=7.2 Hz). Mass Spectrum (LCMS, ESI) calculated for C30H32N3O4 498.2 (M-Boc+H): found 498.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241789B2
Source datasetuspto-grants-2007_07
ORD IDord-ff8d275fb19e45328ee1ab1f8cbfb1ed
Source noteuspto-grants-2007_07