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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591932Generated: October 30, 2026

2-Methoxy-4-(4-methyl-piperazin-1-yl)-benzaldehyde → HCID 178493011, compound

https://huagongshe.com/reaction/591932

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxy-4-(4-methyl-piperazin-1-yl)-benzaldehydeHCID 84008215—
Reactant(1S,2S,3R,4R)-3-(2,3-Diamino-5-chloro-pyridin-4-ylamino)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amideHCID 117701912—
ReactantHCID 178513995HCID 178513995—
ProductHCID 178493011HCID 17849301162%

Reaction Steps

In the same fashion as for Compound III, (1S,2S,3R,4R)-3-(2,3-Diamino-5-chloro-pyridin-4-ylamino)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amide and 2-Methoxy-4-(4-methyl-piperazin-1-yl)-benzaldehyde were reacted to produce the title compound (62%). 1H NMR (d-chloroform): 13.76 (br s, 1H), 8.21 (d, J=8 Hz, 1H), 7.97 (d, J=8 Hz, 1H), 7.80 (s, 1H), 6.62 (d, J=8 Hz, 1H), 6.47 (s, 1H), 6.46 (m, 1H), 6.42 (br s, 1H), 6.07 (br s, 1H), 5.40 (t, J=9 Hz, 1H), 4.11 (s, 3H), 3.65-3.90 (m, 4H), 3.40-3.60 (m, 2H), 3.16 (s, 1H), 3.03 (m, 1H), 2.99 (s, 1H), 2.92 (s, 3H), 2.72) d, J=8 Hz, 1H), 2.32 (d, J=9 Hz, 1H), 1.80-2.10 (m, 2H), 1.68 (d, J=9 Hz, 1H). MS: 509.14 (M+H). HPLC retention time: 1.82 minutes (G Method).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238656B2
Source datasetuspto-grants-2016_01
ORD IDord-d90f85f15ea647eea745f99c7e43d562
Source noteuspto-grants-2016_01