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Sodium Azide → HCID 178488384, compound

HRID 862940
Notes
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Reaction equation

HRID 862940 reaction equation
[Cl-].[Al+3].[Cl-].[Cl-].[N-:5]=[N+:6]=[N-:7].[Na+].[CH3:9][O:10][C:11]1[CH:16]=[CH:15][C:14]([CH:17]2[C:25]3[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=3)[CH:19]([C:26]3[CH:31]=[CH:30][C:29]4[O:32][CH2:33][O:34][C:28]=4[CH:27]=3)[CH:18]2[C:35]#[N:36])=[CH:13][CH:12]=1.[Al](N=[N+]=[N-])(N=[N+]=[N-])N=[N+]=[N-]>C1COCC1>[CH3:9][O:10][C:11]1[CH:16]=[CH:15][C:14]([CH:17]2[C:25]3[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=3)[CH:19]([C:26]3[CH:31]=[CH:30][C:29]4[O:32][CH2:33][O:34][C:28]=4[CH:27]=3)[CH:18]2[C:35]2[NH:36][N:7]=[N:6][N:5]=2)=[CH:13][CH:12]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 33557Sodium AzideHCID 6451240Aluminum(III) ChlorideHCID 16708548HCID 16708548, compoundHCID 18703878HCID 18703878, compound

Product 1

HCID 178488384HCID 178488384, compoundYield 56%

Reagents, catalysts & solvents 1

HCID 8028
Tetrahydrofuran
Solvent
3×

Procedure

To THF (2.5 ml) at -78° C. under an argon atmosphere was added aluminum chloride (90 mg, 0.67 mmol). After slowly warming to room temperature, sodium azide (130 mg, 2.2 mmol) was added, and the resulting mixture was heated at 70° C. for 5 min, then cooled to room temperature. To the reaction mixture was added a solution of (1RS,2SR,3SR)-1-(4-methoxyphenyl)-3-(3,4-methylenedioxyphenyl)indane-2-carbonitrile (125 mg, 0.34 mmol) in THF (2.5 ml). After heating at 70° C. overnight, thin layer chromatographic analysis of the reaction mixture indicated the presence of starting material, so additional Al(N3)3 was prepared as above (1.34 mmol) in THF. To this was added the reaction mixture, and heating at 70° C. was resumed for an additional 5 h. The mixture was partitioned between EtOAc and 3M HCl. The aqueous phase was extracted with EtOAc, and the combined organic extracts were washed successively with H2O and saturated aqueous NaCl and dried. The solvent was removed in vacuo, and the residue was crystallized from EtOAc/hexanes to afford the title compound (78 mg, 56%). A portion of this material was further purified by MPLC (LiChroprep RP-18, MeOH/H2O=60/40) and then recrystallized; m.p. 155°-157° C. (EtOAc/hexanes).

Workup

  1. temperaturethe resulting mixture was heated at 70° C. for 5 min
  2. temperaturecooled to room temperature
  3. temperatureAfter heating at 70° C. overnight
  4. additionTo this was added the reaction mixture
  5. temperatureheating at 70° C.
  6. customThe mixture was partitioned between EtOAc and 3M HCl
  7. extractionThe aqueous phase was extracted with EtOAc
  8. washthe combined organic extracts were washed successively with H2O and saturated aqueous NaCl
  9. customdried
  10. customThe solvent was removed in vacuo
  11. customthe residue was crystallized from EtOAc/hexanes

Sources & evidence

ORD record
ord-64562b038b0142b5916af19f19c5928f
Source dataset
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05719182

Reaction notes

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