Triethylamine → HCID 10187558, compound

HRID 1790646Notes

Reaction equation

HRID 1790646 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

5

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

  1. stirringthe reaction was stirred an additional hour
  2. extractionwas extracted with EtOAc
  3. extractionThen, the organic layer was was extracted with brine
  4. dry with materialThe combined organics were dried with magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. 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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