Hydrochloric Acid → HCID 57448670, compound

HRID 446671Notes

Reaction equation

HRID 446671 reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([S:9]([NH:12][C:13]2[C:22]([NH:23][C:24]3[CH:29]=[C:28]([O:30][CH3:31])[CH:27]=[C:26]([O:32][CH3:33])[CH:25]=3)=[N:21][C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[N:14]=2)(=[O:11])=[O:10])[CH:6]=[CH:7][CH:8]=1)#[N:2].[N-:34]=[N+:35]=[N-:36].[Na+].[Cl-].[NH4+].Cl>CN(C)C=O>[CH3:31][O:30][C:28]1[CH:29]=[C:24]([NH:23][C:22]2[C:13]([NH:12][S:9]([C:5]3[CH:6]=[CH:7][CH:8]=[C:3]([C:1]4[N:34]=[N:35][NH:36][N:2]=4)[CH:4]=3)(=[O:10])=[O:11])=[N:14][C:15]3[C:20]([N:21]=2)=[CH:19][CH:18]=[CH:17][CH:16]=3)[CH:25]=[C:26]([O:32][CH3:33])[CH:27]=1

Participants

6

Procedure

To a stirred solution of 3-cyano-N-(3-(3,5-dimethoxyphenylamino)quinoxalin-2-yl)benzenesulfonamide (0.20 g, 0.44 mmol), prepared using procedures similar to those described in Example 115, in dimethylformamide (1.2 mL) at 50° C. were added sodium azide (0.11 g, 1.76 mmol) and ammonium chloride (94 mg, 1.76 mmol). The crude mixture was heated at 100° C. overnight. The reaction was cooled to room temperature treated with ice water (20 mL) followed by concentrated hydrochloric acid (10 mL). The solid obtained was filtered under reduced pressure and washed with hexane (20 mL), diethyl ether (20 mL), and ethyl acetate (5 mL) to afford N-(3-{[3,5-bis(methoxy)phenyl]amino}quinoxalin-2-yl)-3-(2H-tetrazol-5-yl)benzenesulfonamide (55 mg, 25%) as light yellow solid. MS (EI) m/z for C23H20N8O4S: 505.0 (MH+).

Workup

  1. customThe solid obtained
  2. filtrationwas filtered under reduced pressure
  3. washwashed with hexane (20 mL), diethyl ether (20 mL), and ethyl acetate (5 mL)

Sources & evidence

ORD record
ord-6bbf2ec2accb46d4ac27f5aaa5332c6f
Source dataset
uspto-grants-2013_07
Patent number
US08481001B2

Reaction notes

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