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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095802Generated: October 30, 2026

Hexahydro-1,4-diazepine → 8-(6-(1,4-Diazepan-1-yl)hexyloxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxyquinolin-2(1H)-one

https://huagongshe.com/reaction/1095802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexahydro-1,4-diazepineHCID 68163—
Reactant8-(6-chlorohexyloxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxyquinolin-2(1H)-oneHCID 59268117—
Product8-(6-(1,4-Diazepan-1-yl)hexyloxy)-4-(3,5-dichloropyridin-4-ylamino)-7-methoxyquinolin-2(1H)-oneHCID 53346470—

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 1,4-diazepane following the procedure outlined in Example 18, Step 2 (modifications: 40° C., 8 h). 1H NMR (400 MHz, DMSO-d6): δ 8.68 (s, 2H), 7.85 (d, 1H), 7.00 (d, 1H), 4.69 (s, 1H), 3.95 (t, 2H), 3.88 (s, 3H), 2.79 (t, 2H), 2.74 (m, 2H), 2.60-2.52 (m, 4H), 2.40 (t, 2H), 1.74 (m, 2H), 1.63 (m, 2H), 1.39 (m, 4H), 1.30 (m, 2H) [NH's not seen]; MS (ESI): 534.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138205B2
Source datasetuspto-grants-2012_03
ORD IDord-942141859e6a4f699148c474582ac24d
Source noteuspto-grants-2012_03