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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591935Generated: October 25, 2026

3-(Dimethylamino)benzaldehyde → HCID 178482747, compound

https://huagongshe.com/reaction/591935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Dimethylamino)benzaldehydeHCID 34288—
ReactantHCID 117701849HCID 117701849—
ReactantHCID 178513995HCID 178513995—
ProductHCID 178482747HCID 17848274758%

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-Dimethylamino-benzaldehyde were reacted to produce the title compound (58%). 1H NMR (d-chloroform): 16.03 (br s, 1H), 8.36 (d, J=9 Hz, 1H), 7.82 (s, 1H), 7.74 (s, 1H), 7.61 (d, J=9 Hz, 1H), 7.45 (t, J=8 Hz, 1H), 7.09 (t, J=8 Hz, 1H), 6.50 (m, 1H), 6.42 (m, 1H), 6.04 (m, 1H), 5.69 (m, 1H), 5.37 (t, J=7 Hz, 1H), 3.17 (s, 1H), 3.13 (s, 6H), 3.04 (s, 1H), 2.71 (d, J=9 Hz, 1H), 2.33 (d, J=9 Hz, 1H), 1.68 (d, J=9 Hz, 1H). MS: 423.15 (M+H). HPLC retention time: 2.05 minutes (G Method).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238656B2
Source datasetuspto-grants-2016_01
ORD IDord-4c16454d42d64e0d940bd1a9a6d2df69
Source noteuspto-grants-2016_01