Sodium Azide → HCID 178517237, compound

HRID 1392190Notes

Reaction equation

HRID 1392190 reaction equation
[N-:1]=[N+:2]=[N-:3].[Na+].[C:5]([C:7]1[CH:31]=[CH:30][C:10]([CH2:11][C:12]23[CH2:19][CH2:18][CH2:17][N:16]2[C:15](=[O:20])[N:14]([C:21]2[CH:26]=[C:25]([Cl:27])[CH:24]=[C:23]([Cl:28])[CH:22]=2)[C:13]3=[O:29])=[CH:9][CH:8]=1)#[N:6]>CN(C=O)C>[NH:1]1[C:5]([C:7]2[CH:8]=[CH:9][C:10]([CH2:11][C:12]34[CH2:19][CH2:18][CH2:17][N:16]3[C:15](=[O:20])[N:14]([C:21]3[CH:22]=[C:23]([Cl:28])[CH:24]=[C:25]([Cl:27])[CH:26]=3)[C:13]4=[O:29])=[CH:30][CH:31]=2)=[N:6][N:3]=[N:2]1

Participants

4

Conditions

Temperature
140 °C

Procedure

NaN3 (64.5 mg) was added to a solution of Example 21 (137 mg) in DMF (3 mL). The reaction mixture was sealed and heated at 140° C. for 72 hours. The reaction mixture was cooled to room temperature and the solvent removed under reduced pressure. The residue was purified by HPLC (18C-Waters 40×210 mm, 1% HOAc/CH3CN gradient) to provide the titled compound (27 mg). MS (m/z) 457 (MH+). mp. 194.8° C.

Workup

  1. customThe reaction mixture was sealed
  2. temperatureThe reaction mixture was cooled to room temperature
  3. customthe solvent removed under reduced pressure
  4. customThe residue was purified by HPLC (18C-Waters 40×210 mm, 1% HOAc/CH3CN gradient)

Sources & evidence

ORD record
ord-972e02fd9ab54e2799fdf7aa94e28aca
Source dataset
uspto-grants-2008_03
Patent number
US07342012B2

Reaction notes

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