Sodium Hydroxide → Sodium Azide
Reaction equation
N1C=CC(C2SC=C(C([N:14]=[N+:15]=[N-:16])=O)N=2)=CC=1.[N:17]1[CH:22]=[CH:21][CH:20]=[C:19](C2SC=C(C(O)=O)N=2)[CH:18]=1.[OH-].[Na+:32].C(Cl)(=O)C(Cl)=O>O>[N-:14]=[N+:15]=[N-:16].[Na+:32].[N:17]1[CH:22]=[CH:21][CH:20]=[C:19]([N:14]=[N+:15]=[N-:16])[CH:18]=1Participants
7
Procedure
In a manner similar to that described for the preparation of 2-(4-pyridinyl)-4-thiazolylcarbonylazide, 6.0 g of 2-(3-pyridinyl)-4-thiazolylcarboxylic acid was treated successively with NaOH, oxalyl chloride and a solution of NaN3 in water to give the 3-pyridinylazide as a pale brown solid. MS m/z: 204.5 (M−N2+H)
Sources & evidence
- ORD record
- ord-18497d9952fb4b1c9e176f27df82a737
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06645990B2
Reaction notes
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