1-Hydroxybenzotriazole → HCID 178522663, compound
Reaction equation
[CH:1]1([C:7]2[C:11]([CH2:12][C:13]3[CH:21]=[CH:20][C:16]([C:17](O)=[O:18])=[CH:15][CH:14]=3)=[CH:10][N:9]([C:22]3[CH:27]=[CH:26][C:25]([O:28][C:29]([F:32])([F:31])[F:30])=[CH:24][CH:23]=3)[N:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C1C=CC2N(O)N=NC=2C=1.O.[NH2:44][C:45]1[NH:49][N:48]=[N:47][N:46]=1.CCN(C(C)C)C(C)C>CN(C=O)C.O.C(Cl)CCl>[CH:1]1([C:7]2[C:11]([CH2:12][C:13]3[CH:21]=[CH:20][C:16]([C:17]([NH:44][C:45]4[NH:49][N:48]=[N:47][N:46]=4)=[O:18])=[CH:15][CH:14]=3)=[CH:10][N:9]([C:22]3[CH:23]=[CH:24][C:25]([O:28][C:29]([F:31])([F:32])[F:30])=[CH:26][CH:27]=3)[N:8]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
A mixture of 66.7 mg product from Step B above, 71.9 mg EDC, 30.4 mg HOBt and 23.2 mg aminotetrazole monohydrate was dissolved in 1 mL DMF. DIEA (92 μL) was added immediately and the resulting solution was stirred at room temperature for 17 hours. The reaction mixture was diluted with about 2:1 mixture of DMF and water and purified on preparative HPLC using 70˜80% MeCN gradient over 10 minutes at 8.0 mL per minute with 0.1% TFA. The title compound was obtained as a white solid following lyophilization. 1H NMR (DMSO-d6, 500 MHz) δ 8.26 (s, 1H), 8.02 (d, J=8.2 Hz, 2H), 7.84˜7.87 (m, 2), 7.40˜7.45 (m, 4H), 3.92 (s, 2H), 2.58 (tt, J=3.4 & 11.9 Hz, 1H), 1.62˜1.74 (m, 5H), 1.41˜1.50 (m, 2H), 1.17˜1.31 (m, 3H). LC-MS: 2.41 min. (M+H=512.3).
Workup
- custompurified on preparative HPLC
- customover 10 minutes
Sources & evidence
- ORD record
- ord-0a947de5bdc04026a46f7d9aa81e1018
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07572922B2
Reaction notes
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