4-[(Morpholin-4-yl)methyl]benzaldehyde → HCID 178514010, compound

HRID 591974Notes

Reaction equation

HRID 591974 reaction equation
[NH2:1][C:2]1[C:7]([NH2:8])=[C:6]([NH:9][C@@H:10]2[C@@H:15]3[CH2:16][C@@H:12]([CH:13]=[CH:14]3)[C@@H:11]2[C:17]([NH2:19])=[O:18])[CH:5]=[CH:4][N:3]=1.[N:20]1([CH2:26][C:27]2[CH:34]=[CH:33][C:30]([CH:31]=O)=[CH:29][CH:28]=2)[CH2:25][CH2:24][O:23][CH2:22][CH2:21]1>>[N:20]1([CH2:26][C:27]2[CH:34]=[CH:33][C:30]([C:31]3[NH:1][C:2]4=[N:3][CH:4]=[CH:5][C:6]([NH:9][C@@H:10]5[C@@H:15]6[CH2:16][C@@H:12]([CH:13]=[CH:14]6)[C@@H:11]5[C:17]([NH2:19])=[O:18])=[C:7]4[N:8]=3)=[CH:29][CH:28]=2)[CH2:21][CH2:22][O:23][CH2:24][CH2:25]1

Participants

3

Procedure

In a similar fashion to Compound LXXXVII, (1S,2S,3R,4R)-3-(2,3-Diamino-pyridin-4-ylamino)-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid amide (50.0 mg, 0.193 mmol) and 4-morpholin-4-ylmethyl-benzaldehyde (43.5 mg, 0.212 mmol) were reacted to produce 27 mg (32%) of the title compound. mp: 240-244° C., 1H NMR (300 MHz, DMSO-d6): 13.06 (s, 1H), 8.09 (d, J=8 Hz, 2H), 7.91 (d, 1H), 7.67 (s, 1H), 7.45 (d, J=8 Hz, 1H), 7.16 (s, 1H), 6.88 (m, 1H), 6.41 (d, J=8 Hz, 1H), 6.33 (s, 1H), 3.88 (br s, 1H), 3.59 (br s, 4H), 3.52 (s, 2H), 2.88 (s, 1H), 2.76 (s, 1H), 2.60 (d, J=8 Hz, 1H), 2.38 (s, 4H), 2.23 (d, J=8 Hz, 1H), 1.43 (d, J=8 Hz, 1H). MS: 445 (M+H), HPLC: 1.51 min (G method).

Sources & evidence

ORD record
ord-edb315d9ddff4d38b55ee7e87ea1892a
Source dataset
uspto-grants-2016_01
Patent number
US09238656B2

Reaction notes

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