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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095803Generated: October 31, 2026

1-Methylhomopiperazine → 4-(3,5-Dichloropyridin-4-ylamino)-7-methoxy-8-(6-(4-methyl-1,4-diazepan-1-yl)hexyloxy)quinolin-2(1H)-one

https://huagongshe.com/reaction/1095803

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylhomopiperazineHCID 228349—
Reactant8-(6-chlorohexyloxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxyquinolin-2(1H)-oneHCID 59268117—
Product4-(3,5-Dichloropyridin-4-ylamino)-7-methoxy-8-(6-(4-methyl-1,4-diazepan-1-yl)hexyloxy)quinolin-2(1H)-oneHCID 53346471—

Reaction Steps

The title compound was prepared from 8-(6-chlorohexyloxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxyquinolin-2(1H)-one (Intermediate 4) and 1-methyl-1,4-diazepane following the procedure outlined in Example 18, Step 2 (modifications: 40° C., 24 h). 1H NMR (400 MHz, DMSO-d6): δ 9.93 (s, 1H), 8.82 (br, 1H), 8.75 (s, 2H), 7.87 (d, 1H), 7.04 (d, 1H), 4.76 (s, 1H), 3.95 (t, 2H), 3.89 (s, 3H), 2.62-2.42 (m, 8H), 2.37 (t, 2H), 2.21 (s, 3H), 1.74 (m, 2H), 1.66 (m, 2H), 1.38 (m, 4H), 1.29 (m, 2H); MS (ESI): 548.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138205B2
Source datasetuspto-grants-2012_03
ORD IDord-72f1c7a3c5a242449a08fa14a55521da
Source noteuspto-grants-2012_03