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1,2-Dichloroethane → HCID 136337174, compound

HRID 1428848
Notes
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Reaction equation

HRID 1428848 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][N:9]([C:11](=[N:18][C:19]2[CH:24]=[C:23]([F:25])[CH:22]=[C:21]([F:26])[CH:20]=2)[NH:12][C:13](OCC)=[O:14])[CH:10]=1)=[O:5])[CH3:2].ClCCCl.O.CO>[Ti](Cl)(Cl)(Cl)Cl.C(Cl)Cl>[CH2:1]([O:3][C:4]([C:6]1[CH:7]=[N:8][N:9]([C:11]2[NH:12][C:13](=[O:14])[C:24]3[C:19](=[CH:20][C:21]([F:26])=[CH:22][C:23]=3[F:25])[N:18]=2)[CH:10]=1)=[O:5])[CH3:2]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 111,2-DichloroethaneHCID 887MethanolHCID 962WaterHCID 136337173HCID 136337173, compound

Product 1

HCID 136337174HCID 136337174, compoundYield 61.3%

Reagents, catalysts & solvents 2

HCID 24193
Titanium Tetrachloride
Catalyst
HCID 6344DichloromethaneSolvent

Conditions

Temperature
110 °C

Procedure

Titanium (IV) chloride (0.39 mL, 3.5 mmol) was carefully added to a solution of 1-[(3,5-difluoro-phenylimino)-ethoxycarbonylamino-methyl]-1H-pyrazole-4-carboxylic acid ethyl ester (0.321 g, 0.876 mmol) and DCE (2.7 mL), and the resulting solution was heated to 110° C. for 1.5 h. The reaction mixture was cooled to room temperature and water (50 mL), methanol (1 mL), and DCM (40 mL) were added. The biphasic mixture was stirred for 30 min, and the layers were separated. The aqueous layer was further extracted with DCM (2×30 mL). The combined organic layers were washed with brine (40 mL), dried (MgSO4), and concentrated. The residue was triturated from EtOH to yield the titled compound (0.172 g, 60% yield). MS (ESI/Cl): mass calcd. for C14H10F2N4O3, 320.1; m/z found, 321.1 [M+H]+. 1H NMR (400 MHz, DMSO-d6): 13.09 (s, 1H), 8.99 (d, J=0.5 Hz, 1H), 8.35 (s, 1H), 7.42-7.32 (m, 2H), 4.30 (q, J=7.1 Hz, 2H), 1.32 (t, J=7.1 Hz, 3H).

Workup

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customthe layers were separated
  3. extractionThe aqueous layer was further extracted with DCM (2×30 mL)
  4. washThe combined organic layers were washed with brine (40 mL)
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated
  7. customThe residue was triturated from EtOH

Sources & evidence

ORD record
ord-0897ad8ba2104191adec3a0e547b0057
Source dataset
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08937078B2

Reaction notes

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