Triethylamine → HCID 10187558, compound
Reaction equation
[CH3:1][CH:2]([CH3:39])[CH2:3][C@H:4]([NH:26][C:27]([C:29]1[CH:30]=[C:31]2[C:36](=[CH:37][CH:38]=1)[N:35]=[CH:34][CH:33]=[CH:32]2)=[O:28])[C:5](=[O:25])[NH:6][C@H:7]1[CH2:13][CH2:12][C@@H:11]([CH3:14])[N:10]([S:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][N:19]=2)(=[O:17])=[O:16])[CH2:9][CH:8]1[OH:24].C(N(CC)CC)C>CS(C)=O.O>[CH3:1][CH:2]([CH3:39])[CH2:3][C@H:4]([NH:26][C:27]([C:29]1[CH:30]=[C:31]2[C:36](=[CH:37][CH:38]=1)[N:35]=[CH:34][CH:33]=[CH:32]2)=[O:28])[C:5](=[O:25])[NH:6][C@H:7]1[CH2:13][CH2:12][C@@H:11]([CH3:14])[N:10]([S:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][N:19]=2)(=[O:17])=[O:16])[CH2:9][C:8]1=[O:24]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Sulfur trioxide-pyridine complex (11 mg, 0.7 mmol) was added to a solution of quinoline-6-carboxylic acid {(S)-3-methyl-1-[(4S,7R)-7-methyl-3-hydroxy-1-(pyridine-2-sulfonyl)-azepan-4-ylcarbamoyl]-butyl}-amide (130 mg, 0.235 mmol) in DMSO (2.0 ml) and triethylamine (0.2 ml, 1.4 mmol) was stirred at RT for 1 h. The reaction was incomplete; therefore, additional triethyl amine (0.2 ml, 1.4 mmol) and sulfur trioxide-pyridine complex (11 mg, 0.7 mmol) was added and the reaction was stirred an additional hour. The reaction mixture was diluted with water, then was extracted with EtOAc. Then, the organic layer was was extracted with brine. The combined organics were dried with magnesium sulfate, filtered, concentrated in vacuo, and purified by column chromatography (3% MeOH/CH2Cl2) gave the title compound (100 mg, 77%): 1H NMR:9.0 (sm 1H), 8.70 (s, 1H), 7.90–8.30 (m, 6H), 7.50–7.55 (m, 2H), 7.10 (d, 1H), 7.0 (d, 1H), 5.10–5.15 (m, 1H), 4.70–4.80 (m,2H), 4.35–4.40 (m, 1H), 3.85 (d, 1H), 2.0–2.25 (m, 3H), 1.70–1.80 (m, 2H), 1.60–1.70 (m, 2H), 0.90–1.10 (m, 9H); Electrospray mass spec: M+H+=552.4.
Workup
- stirringthe reaction was stirred an additional hour
- extractionwas extracted with EtOAc
- extractionThen, the organic layer was was extracted with brine
- dry with materialThe combined organics were dried with magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- custompurified by column chromatography (3% MeOH/CH2Cl2)
Sources & evidence
- ORD record
- ord-f3aed56474904f15b2a89ffb12cde371
- Source dataset
- uspto-grants-2006_07
- Patent number
- US07071184B2
Reaction notes
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