Ammonium Chloride → HCID 178439360, compound

HRID 347510Notes

Reaction equation

HRID 347510 reaction equation
[F:1][C:2]1[CH:20]=[C:19]([N+:21]([O-])=O)[CH:18]=[CH:17][C:3]=1[O:4][CH:5]1[C:10]2=[C:11]([CH:14]([CH3:16])[CH3:15])[CH:12]=[CH:13][N:9]2[N:8]=[CH:7][NH:6]1.[Cl-].[NH4+]>[Zn].CO.O1CCCC1>[F:1][C:2]1[CH:20]=[C:19]([NH2:21])[CH:18]=[CH:17][C:3]=1[O:4][CH:5]1[C:10]2=[C:11]([CH:14]([CH3:15])[CH3:16])[CH:12]=[CH:13][N:9]2[N:8]=[CH:7][NH:6]1

Participants

5

Procedure

To a heterogeneous mixture of 4-(2-fluoro-4-nitrophenoxy)-5-isopropyl-3,4-dihydropyrrolo[2,1-f][1,2,4]triazine (0.044 g, 1.39 mmol, 10 equiv) in 1/1 anhydrous methanol/tetrahydrofuran (2 mL), at ambient temperature under nitrogen atmosphere, was added zinc dust (0.090 g, 0.139 mmol, 1.0 equiv) and ammonium chloride (0.075 g, 1.39 mmol, 10 equiv). The mixture was stirred for 4 h before the catalyst was filtered off and the filtrate was concentrated in vacuo to yield the title compound (0.040 g, 100%) as a solid, that was used without further purification. HRMS(ESI), 287.1308 (M+H)+ calc, 287.1300 (M+H)+ found.

Workup

  1. filtrationwas filtered off
  2. concentrationthe filtrate was concentrated in vacuo

Sources & evidence

ORD record
ord-6fecd77714c646f899d19fc041361d8d
Source dataset
uspto-grants-2007_02
Patent number
US07173031B2

Reaction notes

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