Triethylamine → 1-[3-[(N-Ethylpyrrolidin-2-ylmethyl)carbamoyl]phenyl carbamoyl]-5-methylthio-6-trifluoromethyl indoline

HRID 1740810Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1740810
[CH3:1][S:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[C:12]([F:15])([F:14])[F:13])[N:8]([C:16](=[O:27])[NH:17][C:18]1[CH:23]=[CH:22][CH:21]=[C:20]([C:24](O)=[O:25])[CH:19]=1)[CH2:7][CH2:6]2.C(Cl)(=O)C(Cl)=O.C(N(CC)CC)C.[CH2:41]([N:43]1[CH2:47][CH2:46][CH2:45][CH:44]1[CH2:48][NH2:49])[CH3:42]>ClCCl.C1COCC1.CN(C=O)C>[CH2:41]([N:43]1[CH2:47][CH2:46][CH2:45][CH:44]1[CH2:48][NH:49][C:24]([C:20]1[CH:19]=[C:18]([NH:17][C:16]([N:8]2[C:9]3[C:5](=[CH:4][C:3]([S:2][CH3:1])=[C:11]([C:12]([F:13])([F:15])[F:14])[CH:10]=3)[CH2:6][CH2:7]2)=[O:27])[CH:23]=[CH:22][CH:21]=1)=[O:25])[CH3:42]

Komponenten

8

Versuchsvorschrift

The carboxylic acid from Example 12 (0.5 g, 1.25 mol) in dichloromethane (10 ml) was treated with oxalyl chloride (6.3 ml, 3.4 mmol) and DMF (catalytic). The solution was stirred for 1 hour and evaporated to dryness. The residue in dry THF (5 ml) was added to a stirred solution of triethylamine (0.3 ml, 4 mmol) and N-Ethyl-2-aminomethyl pyrrolidine (0.57 g, 4.5 mmol). After 3 hours at room temperature the solution was partitioned (EtOAc/H2O). Drying and removal of organics followed by rexst (EtOAc/60°-80° C. petrol) afforded the title compound as a white powder, m.pt. 174°-175° C.

Aufarbeitung

  1. customevaporated to dryness
  2. customAfter 3 hours at room temperature the solution was partitioned (EtOAc/H2O)
  3. customDrying
  4. customremoval
  5. customof organics followed by rexst (EtOAc/60°-80° C. petrol)

Quellen und Nachweise

ORD-Eintrag
ord-e5e91b3376fa42d481c7301bb084e620
Quelldatensatz
uspto-grants-1999_10
Patentnummer
US05972937

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