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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591943Generated: November 1, 2026

2-Methoxy-4-morpholin-4-yl-benzaldehyde → HCID 178493033, compound

https://huagongshe.com/reaction/591943

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxy-4-morpholin-4-yl-benzaldehydeHCID 976800—
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 178493033HCID 17849303365%

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-morpholin-4-yl-benzaldehyde were reacted to produce the title compound (65%). 1H NMR (d-chloroform): 13.88 (br s, 1H), 8.25 (m, 2H), 7.77 (s, 1H), 7.18 (s, 1H), 7.07 (d, J=7 Hz, 1H), 6.42 (m, 3H), 5.81 (s, 1H), 5.29 (t, J=7 Hz, 1H), 4.53 (d, J=9 Hz, 1H), 4.10-3.94 (m, 10H), 3.68 (m, 1H), 3.35 (m, 1H), 3.16 (s, 1H), 2.92 (s, 1H), 2.77 (d, J=8 Hz, 1H), 2.38 (d, J=9 Hz, 1H), 1.63 (d, J=9 Hz, 1H). MS: 509.16 (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-12a81a5a11274f2d83879c549234ee2b
Source noteuspto-grants-2016_01