Sodium Azide → HCID 15220953, compound
Reaction equation
[CH2:1]([O:8][C:9]1[CH:17]=[CH:16][C:12](C(O)=O)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:18](Cl)(=[O:22])C(Cl)=O.[N-:24]=[N+]=[N-].[Na+].[C:28]1([CH:34]2[CH:38]([C:39]3[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=3)[NH:37][NH:36][C:35]2=[O:45])[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>C1(C)C=CC=CC=1.O>[CH2:1]([O:8][C:9]1[CH:10]=[CH:11][C:12]([NH:24][C:18]([N:37]2[CH:38]([C:39]3[CH:40]=[CH:41][CH:42]=[CH:43][CH:44]=3)[CH:34]([C:28]3[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=3)[C:35](=[O:45])[NH:36]2)=[O:22])=[CH:16][CH:17]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
Procedure
4-Benzyloxybenzoic acid (2.0 g, 8.8 mmol) was suspended in 50 mL toluene with oxalyl chloride (5 mL) and heated to reflux for 15 min. Solvent was removed in vacuo, the residue redissolved in 30 mL acetone, and an aqueous solution of NaN3 (1.16 g, 17.6 mmol, 2.0 eq. in 10 mL H2O) added dropwise with external cooling by a water bath. The mixture was stirred for 1 hour, diluted with H2O, extracted twice with toluene, then the combined extracts washed with water and brine, and dried over Na2SO4. This solution of acyl azide was treated with 4,5-diphenyl-3-pyrazolidinone (1.6 g, 6.8 mmol, 0.76 eq.), warmed until bubbles evolved, and heating maintained for 30 min. After stirring overnight at room temperature, the solvent was removed in vacuo, and the product isolated by chromatography (0-30% EtOAc:hexane gradient) as 1.6 g (52%) white solid: mp 127°-30° C.;
Workup
- temperatureheated
- temperatureto reflux for 15 min
- customSolvent was removed in vacuo
- dissolutionthe residue redissolved in 30 mL acetone
- temperaturewith external cooling by a water bath
- extractionextracted twice with toluene
- washthe combined extracts washed with water and brine
- dry with materialdried over Na2SO4
- temperaturewarmed until bubbles
- temperatureheating
- temperaturemaintained for 30 min
- stirringAfter stirring overnight at room temperature
- customthe solvent was removed in vacuo
Sources & evidence
- ORD record
- ord-bc29a0d1f66f480ab7e235039c63e8a1
- Source dataset
- uspto-grants-1994_04
- Patent number
- US05300514
Reaction notes
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