Hydroxyamine hydrochloride → HCID 11120992, compound
Reaction equation
[Br:1][C:2]1[CH:18]=[CH:17][C:5]([C:6]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14](O)=[O:15])=[O:7])=[CH:4][CH:3]=1.[NH2:19][OH:20].Cl>C(N(CC)CC)C>[OH:20][NH:19][C:14](=[O:15])[CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][C:6](=[O:7])[C:5]1[CH:17]=[CH:18][C:2]([Br:1])=[CH:3][CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Following the procedure described in Example 14, step 3, but substituting carboxylic acid 50d for 37 and using 1.1 equivalent of NH2OH.HCl and triethylamine each, the title compound was obtained as light yellow solid in 31% yield: 1H NMR (300 MHz, CD3OD/CDCl3=5/1) δ 7.82 (d, J=7.5 Hz, 2H), 7.62 (d, J=7.5 Hz, 2H), 2.95 (t, J=7.2 Hz, 2H), 2.11 (m, 2H), 1.55-1.79 (m, 4H), 1.38 (m, 4H).
Sources & evidence
- ORD record
- ord-bf8841593b5d410b891df2385b331409
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07288567B2
Reaction notes
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