Carbon Dioxide → HCID 70154371, compound

HRID 2187429Notes

Reaction equation

[N:1]1([C:7]2[CH:15]=[CH:14][C:10]([C:11]([OH:13])=O)=[CH:9][CH:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C(N1C=CN=C1)([N:18]1C=CN=C1)=O.C(=O)=O.N[C@@H:32]1[CH2:41][CH2:40][C:39]2[C:34](=[C:35]([N:42]3[CH2:47][CH2:46][N:45]([CH3:48])[CH2:44][CH2:43]3)[CH:36]=[CH:37][CH:38]=2)[CH2:33]1>CN(C)C=O>[CH3:48][N:45]1[CH2:44][CH2:43][N:42]([C:35]2[CH:36]=[CH:37][CH:38]=[C:39]3[C:34]=2[CH2:33][C@H:32]([C:9]2[CH:8]=[C:7]([N:1]4[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]4)[CH:15]=[CH:14][C:10]=2[C:11]([NH2:18])=[O:13])[CH2:41][CH2:40]3)[CH2:47][CH2:46]1

Participants

Conditions

Temperature: 75 °C

Procedure

To a solution of 4-piperidinobenzoic acid (88 mg, 0.43 mmol; described in: Weringa, W. D.; Janssen, M. J. Recl. Trav. Chim. Pays-Bas 1968, 87(12), 1372-1380) in anhydrous N,N-dimethylformamide (5 mL) was added 1,1′-carbonyldiimidazole (73 mg, 0.45 mmol) and the reaction was heated at 75° C. When the carbon dioxide evolution had ceased (after 30 min), the reaction was cooled to room temperature and a solution of (R)-2-amino-8-(4-methylpiperazin-1-yl)-1,2,3,4-tetrahydronaphthalene (100 mg, 0.41 mmol) in anhydrous N,N-dimethylformamide (5 mL) was added. The reaction was allowed to stir at ambient temperature for 17 h and the solvent was evaporated in vacuo. Purification on a silica gel column using chloroform/ethanol saturated with NH3 (100:2) as the eluent gave 75 mg (42% yield) of the title compound as white crystals: mp 196-198° C.; [α]21D '63° (c 1.0, chloroform); EIMS (70 eV) m/z (relative intensity) 432 (2, M+).

Workup

custom(after 30 min)
temperaturethe reaction was cooled to room temperature
customthe solvent was evaporated in vacuo
customPurification on a silica gel column

Sources & evidence

ORD record: ord-3641e56f93ee47cb8d844e9f46967c6c
Source dataset: uspto-grants-2002_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06410530B1

Reaction notes

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