HCID 67447598, compound → HCID 178520034, compound
Reaction equation
[O:1]=[C:2]1[C@@:10]2([CH2:12][C@H:11]2[C:13]2[CH:21]=[C:20]3[C:16]([C:17]([C:22]#N)=[N:18][NH:19]3)=[CH:15][CH:14]=2)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[NH:3]1.[PH2]([O-])=[O:25].[Na+]>N1C=CC=CC=1.O.[Ni]>[O:1]=[C:2]1[C@@:10]2([CH2:12][C@H:11]2[C:13]2[CH:21]=[C:20]3[C:16]([C:17]([CH:22]=[O:25])=[N:18][NH:19]3)=[CH:15][CH:14]=2)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[NH:3]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Procedure
To a solution of 6-((1R*,2S*)-2′-oxospiro[cyclopropane-1,3′-indoline]-2-yl)-1H-indazole-3-carbonitrile (1 g, 3.3 mmol) in pyridine (30 mL) acetic acid (8 mL) and water (8 mL) and Raney Nickel (1 g). Sodium hypophosphite (1.8 g, 21 mmol) was dissolved in water (10 mL) and added dropwise and the reaction was stirred overnight. The product was extracted into ethyl acetate (300 mL), washed with brine (50 mL), dried over MgSO4 and concentrated to dryness. The residue was purified by silica gel chromatography (95:5 CH2Cl2/MeOH) to give the title compound as a yellow solid (300 mg, 30%). 1H NMR (400 MHz, CD3OD) δ 10.17 (s, 1H), 8.10 (d, J=8.3 Hz, 1H), 7.55 (s, 1H), 7.17 (d, J=8.5 Hz, 1H) 7.08-7.04 (m, 1H), 6.94 (d, J=8.3 Hz, 1H), 6.56 (t, J=7.6 Hz, 1H), 5.93 (d, J=7.5 Hz, 1H), 3.38-3.34 (m, 1H), 2.27-2.17 (m, 1H).
Workup
- additionadded dropwise
- extractionThe product was extracted into ethyl acetate (300 mL)
- washwashed with brine (50 mL)
- dry with materialdried over MgSO4
- concentrationconcentrated to dryness
- customThe residue was purified by silica gel chromatography (95:5 CH2Cl2/MeOH)
Sources & evidence
- ORD record
- ord-50fdada349f84542a8784451aa19a90d
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09139563B2
Reaction notes
Loading…