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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591933Generated: October 30, 2026

2-Methoxy-4-(4-morpholin-4-yl-piperidin-1-yl)-benzaldehyde → HCID 178492999, compound

https://huagongshe.com/reaction/591933

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxy-4-(4-morpholin-4-yl-piperidin-1-yl)-benzaldehydeHCID 117701815—
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 178492999HCID 17849299975%

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-morpholin-4-yl-piperidin-1-yl)-benzaldehyde were reacted to produce the title compound (75%). 1H NMR (d-6 DMSO): 12.50 (br s, 1H), 9.85 (br s, 1H), 8.09 (s, 1H), 8.04 (d, J=9 Hz, 1H), 7.83 (br s, 1H), 7.29 (s, 1H), 6.77 (d, J=9 Hz, 1H), 6.66 (s, 1H), 6.38 (s, 2H), 5.15 (m, 1H), 3.95-4.30 (m, 7H), 3.69 (t, J=10 Hz, 2H), 3.48 (m, 3H), 3.13 (m, 2H), 2.82-2.96 (m, 4H), 2.63 (d, J=8 Hz, 1H), 2.11-2.26 (m, 3H), 2.08 (s, 1H), 1.69 (m, 2H), 1.41 (d, J=9 Hz, 1H). MS: 579.20 (M+H). HPLC retention time: 1.91 minutes (G Method).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238656B2
Source datasetuspto-grants-2016_01
ORD IDord-36ec7056183b475b9832a54936f9557f
Source noteuspto-grants-2016_01