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Water → 1-{1-[(4-Cyclohexylphenyl)carbonyl]azetidin-3-yl}-4-(phenylcarbonyl)-piperazine

HRID 1852571
Notes
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Reaction equation

HRID 1852571 reaction equation
[CH:1]1([C:7]2[CH:12]=[CH:11][C:10]([C:13]([N:15]3[CH2:18][CH:17]([N:19]4[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]4)[CH2:16]3)=[O:14])=[CH:9][CH:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.CN(C(ON1N=N[C:35]2[CH:36]=[CH:37][CH:38]=N[C:34]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[CH3:49]CN(C(C)C)C(C)C.O.CN([CH:62]=[O:63])C>>[CH:1]1([C:7]2[CH:8]=[CH:9][C:10]([C:13]([N:15]3[CH2:18][CH:17]([N:19]4[CH2:20][CH2:21][N:22]([C:62]([C:34]5[CH:35]=[CH:36][CH:37]=[CH:38][CH:49]=5)=[O:63])[CH2:23][CH2:24]4)[CH2:16]3)=[O:14])=[CH:11][CH:12]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 962WaterHCID 6228DimethylformamideHCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 59626057(4-Cyclohexyl-phenyl)-(3-piperazin-1-yl-azetidin-1-yl)-methanone

Product 1

HCID 49763155
1-{1-[(4-Cyclohexylphenyl)carbonyl]azetidin-3-yl}-4-(phenylcarbonyl)-piperazine

Procedure

To a solution of compound 1j (0.08 g, 0.24 mmol) and HATU (0.093 g, 0.24 mmol) in DMF (3 mL) was added DIPEA (0.1 mL). The mixture was stirred at room temperature for 30 min, and then compound 1k (0.03 g, 0.25 mmol) was added to the mixture. The reaction mixture was stirred at room temperature for 18 h. Water (6 mL) was added to the mixture. The mixture was extracted with EtOAc (2×6 mL). The organic layer was dried over MgSO4, filtered, and concentrated. The crude compound 1 was purified by reverse phase chromatography. 1H NMR (300 MHz, CD3OD): δ 7.58 (d, 2H), 7.44-7.53 (m, 5H), 7.34 (d, 2H), 4.6 (m, 1H), 4.42 (m, 2H), 4.27 (m, 1H), 3.85 (m, 5H), 3.05 (m, 4H), 2.57 (m, 1H), 1.85 (m, 5H), 1.45 (m, 5H). MS m/z (M+H+) 432.3.

Workup

  1. stirringThe reaction mixture was stirred at room temperature for 18 h
  2. extractionThe mixture was extracted with EtOAc (2×6 mL)
  3. dry with materialThe organic layer was dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude compound 1 was purified by reverse phase chromatography

Sources & evidence

ORD record
ord-7102f9b1a6e2428da2d617df4eed0fcb
Source dataset
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08962607B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes