Hydrazine → HCID 58204625, compound

HRID 1629406Notes

Reaction equation

HRID 1629406 reaction equation
[CH:1]([N:4]1[C:8]([C:9]2[N:10]=[C:11]3[C:17]4[CH:18]=[CH:19][C:20]([CH:22]([C:28]([O:30]CC)=O)[C:23]([O:25]CC)=O)=[CH:21][C:16]=4[O:15][CH2:14][CH2:13][N:12]3[CH:33]=2)=[N:7][CH:6]=[N:5]1)([CH3:3])[CH3:2].[NH2:34][NH2:35]>C(O)C>[CH:1]([N:4]1[C:8]([C:9]2[N:10]=[C:11]3[C:17]4[CH:18]=[CH:19][C:20]([CH:22]5[C:28](=[O:30])[NH:35][NH:34][C:23]5=[O:25])=[CH:21][C:16]=4[O:15][CH2:14][CH2:13][N:12]3[CH:33]=2)=[N:7][CH:6]=[N:5]1)([CH3:2])[CH3:3]

Participants

4

Reactant 2

HCID 9321HydrazineHCID 67050763HCID 67050763, compound

Product 1

HCID 58204625HCID 58204625, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
75 °C

Procedure

A mixture of 181 mg (0.40 mmol) of diethyl 2-(2-(1-isopropyl-1H-1,2,4-triazol-5-yl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepin-9-yl)malonate and 0.314 mL (10.0 mmol) of hydrazine in 4.0 ml of Ethanol was heated at 75° C. for 18 hours. The mixture was concentrated, the residue triturated with acetic acid. A precipitate was filtered off, washed with acetic acid, ethyl ether and recrystallized from ethyl ether/ethanol mixture to give 360. Yield 59 mg (37.5%). M/z 394.1, calc. 393.15. 1H NMR (400 MHz, DMSO) δ 10.20 (s, 2H), 8.29 (d, J=8.6, 1H), 7.89 (d, J=12.9, 2H), 7.70 (d, J=8.5, 1H), 7.63 (s, 1H), 5.93 (dt, J=13.1, 6.7, 1H), 4.48 (d, J=7.2, 4H), 1.49 (d, J=6.6, 6H)

Workup

  1. concentrationThe mixture was concentrated
  2. customthe residue triturated with acetic acid
  3. filtrationA precipitate was filtered off
  4. washwashed with acetic acid, ethyl ether
  5. customrecrystallized from ethyl ether/ethanol mixture

Sources & evidence

ORD record
ord-224098a389154070aca17d0969d168a0
Source dataset
uspto-grants-2014_07
Patent number
US08785626B2

Reaction notes

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