Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591936Generated: October 26, 2026

3-Morpholinobenzaldehyde → HCID 178513994, compound

https://huagongshe.com/reaction/591936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MorpholinobenzaldehydeHCID 7164584—
ReactantHCID 117701849HCID 117701849—
ReactantHCID 178513995HCID 178513995—
ProductHCID 178513994HCID 17851399411%

Reaction Steps

In the same fashion as for Compound III, (1R,2R,3S,4S)-3-(2,3-Diamino-5-chloro-pyridin-4-ylamino)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amide and 3-Morpholin-4-yl-benzaldehyde were reacted to produce the title compound (11%). 1H NMR (d-chloroform): 16.12 (br s, 1H), 8.42 (d, J=9 Hz, 1H), 7.83 (s, 1H), 7.74 (s, 1H), 7.64 (d, J=8 Hz, 1H), 7.44 (t, J=8 Hz, 1H), 7.07 (d, J=8 Hz, 1H), 6.50 (m, 1H), 6.42 (m, 1H), 5.90 (br s, 1H), 5.65 (br s, 1H), 5.40 (t, J=8 Hz, 1H), 3.94 (m, 4H), 3.34 (m, 4H), 3.18 (s, 1H), 3.07 (s, 1H), 2.69 (d, J=8 Hz, 1H), 2.33 (d, J=9 Hz, 1H), 1.69 (d, J=9 Hz, 1H). MS: 465.15 (M+H). HPLC retention time: 2.39 minutes (G Method).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238656B2
Source datasetuspto-grants-2016_01
ORD IDord-e16fd28cf8f94629afc314f92bc5ad4f
Source noteuspto-grants-2016_01