Water → HCID 178509491, compound
Reaction equation
[NH2:1][C:2]1[C:10]2[C:5](=[N:6][C:7]([CH2:11][N:12]=[N+]=[N-])=[CH:8][CH:9]=2)[NH:4][N:3]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O>C1COCC1>[NH2:1][C:2]1[C:10]2[C:5](=[N:6][C:7]([CH2:11][NH2:12])=[CH:8][CH:9]=2)[NH:4][N:3]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 3-amino-6-azidomethyl-7-azaindazole (60 mg, 0.317 mmol), triphenylphosphine (416 mg, 1.59 mmol) and water (86 mg, 4.76 mmol) in THF (10 mL) was stirred for 64 h. The solvent was evaporated in vacuo and the residue was purified by chromatography on silica (chloroform/ammonia, methanol gradient, 5-10% methanol) to give the title compound as a yellow solid:
Workup
- customThe solvent was evaporated in vacuo
- customthe residue was purified by chromatography on silica (chloroform/ammonia, methanol gradient, 5-10% methanol)
Sources & evidence
- ORD record
- ord-ee08a80d2e0b4893b2f2a0d0708dda4c
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06376499B1
Reaction notes
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