Azido(trimethyl)stannane → HCID 178456811, compound

HRID 612789Notes

Reaction equation

HRID 612789 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]1[CH:14]=[CH:13][C:12]([CH2:15][N:16]2[C:20]3[C:21]([C:25]([O:27][CH2:28][CH3:29])=[O:26])=[CH:22][CH:23]=[CH:24][C:19]=3[N:18]=[C:17]2[NH:30][CH2:31][CH2:32][CH3:33])=[CH:11][CH:10]=1)#[N:2].C[Sn]([N:38]=[N+:39]=[N-:40])(C)C>C1(C)C=CC=CC=1>[CH2:31]([NH:30][C:17]1[N:16]([CH2:15][C:12]2[CH:11]=[CH:10][C:9]([C:4]3[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=3[C:1]3[NH:40][N:39]=[N:38][N:2]=3)=[CH:14][CH:13]=2)[C:20]2[C:21]([C:25]([O:27][CH2:28][CH3:29])=[O:26])=[CH:22][CH:23]=[CH:24][C:19]=2[N:18]=1)[CH2:32][CH3:33]

Participants

4

Procedure

A solution of ethyl 1-[(2'-cyanobiphenyl-4-yl)methyl]-2-propylaminobenzimidazole-7-carboxylate (1.20 g) and trimethyltin azide (2.7 g) in toluene (15 ml) was heated for 50 hours under reflux. Precipitates were collected by filtration and suspended in methanol (20 ml). After addition of 1N-HCl (15 ml), the reaction mixture was stirred at room temperature for 10 minutes. The mixture was adjusted to about pH 5 with 1N-NaOH, followed by extraction with chloroform. The organic layer was washed with water, dried and concentrated to dryness. The concentrate was purified by column chromatography on silica gel to give crystals. Recrystallization from methanol--ethyl acetate gave colorless crystals (10 g, 77%), m.p. 170-172° C.

Workup

  1. temperatureunder reflux
  2. customPrecipitates
  3. filtrationwere collected by filtration
  4. additionAfter addition of 1N-HCl (15 ml)
  5. extractionfollowed by extraction with chloroform
  6. washThe organic layer was washed with water
  7. customdried
  8. concentrationconcentrated to dryness
  9. customThe concentrate was purified by column chromatography on silica gel
  10. customto give crystals
  11. customRecrystallization from methanol

Sources & evidence

ORD record
ord-5277cafa603b48b5bfa30890fdf83467
Source dataset
uspto-grants-1999_12
Patent number
US06004989

Reaction notes

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