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Chloroform → Ethyl Acetate

HRID 131137
Notes
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Reaction equation

HRID 131137 reaction equation
C(N1[CH:12]=[CH:11]N=C1)(N1C=CN=C1)=O.[N:13]1([C:21]2[CH:29]=[CH:28][C:24]([C:25]([OH:27])=[O:26])=[CH:23][CH:22]=2)[CH2:19][CH2:18][C:17](=[O:20])[NH:16][CH2:15][CH2:14]1.[NH2:30][C@H:31]1[CH2:36][C:35]2[C:37]([N:41]3[CH2:46][CH2:45][N:44]([CH3:47])[CH2:43][CH2:42]3)=[CH:38][CH:39]=[CH:40][C:34]=2[O:33][CH2:32]1.C(Cl)(Cl)Cl>CN(C)C=O.C(O)C>[C:25]([O:27][CH2:11][CH3:12])(=[O:26])[CH3:24].[CH3:47][N:44]1[CH2:45][CH2:46][N:41]([C:37]2[C:35]3[CH2:36][C@H:31]([NH:30][C:25](=[O:27])[C:24]4[CH:23]=[CH:22][C:21]([N:13]5[CH2:19][CH2:18][C:17](=[O:20])[NH:16][CH2:15][CH2:14]5)=[CH:29][CH:28]=4)[CH2:32][O:33][C:34]=3[CH:40]=[CH:39][CH:38]=2)[CH2:42][CH2:43]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 6212ChloroformHCID 682631,1'-CarbonyldiimidazoleHCID 11139461(S)-3-amino-5-(4-methylpiperazin-1-yl)-1,4-dihydro-2H-1-benzopyranHCID 220640304-(5-Oxo-1,4-diazepan-1-YL)benzoic acid

Product 2

HCID 8857Ethyl AcetateYield 204.2%
HCID 22896527
HCID 22896527, compound

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 6228DimethylformamideSolvent2×

Procedure

A solution of 1,1′-carbonyldiimidazole (151 mg, 0.934 mmol) and 4-(hexahydro-1,4-diazepin-5-on-1-yl)benzoic acid (219 mg, 0.934 mmol) in anhydrous N,N-dimethylformamide (7 mL) was stirred at 75° C. for 55 min. The mixture was allowed to cool, and a solution of (S)-3-amino-5-(4-methylpiperazin-1-yl)-3,4-dihydro-2H-1-benzopyran (210 mg, 0.85 mmol) in N,N-dimethylformamide (3.5 mL) was added. The reaction mixture was stirred at room temperature for 14 days. The solvent was removed in vacuo, and the residue was purified by column chromatography on silica (eluent: chloroform/ethanol, 90:10+1% conc. NH3). The product was crystallized from a mixture of chloroform, ethanol, and ethyl acetate affording 84 mg (21% yield) of the title compound as white crystals: mp 244-247° C. (decomposes); [α]21D −148° (c 0.50, chloroform); TSPMS (70 eV) m/z 464 (M+1).

Workup

  1. temperatureto cool
  2. customThe solvent was removed in vacuo
  3. customthe residue was purified by column chromatography on silica (eluent: chloroform/ethanol, 90:10+1% conc. NH3)

Sources & evidence

ORD record
ord-0ff41c4ef21a49b78413ad8fb00638df
Source dataset
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07384943B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes