Triethylamine → HCID 18175008, compound

HRID 351145Notes

Reaction equation

HRID 351145 reaction equation
[C:1]([NH:4][CH2:5][CH2:6][C:7]1[CH:8]=[CH:9][CH:10]=[C:11]2[C:16]=1[CH:15]=[C:14]([S:17](Cl)(=[O:19])=[O:18])[CH:13]=[CH:12]2)(=[O:3])[CH3:2].C([N:23](CC)CC)C.[OH-].[NH4+]>C(Cl)Cl>[NH2:23][S:17]([C:14]1[CH:15]=[C:16]2[C:11]([CH:10]=[CH:9][CH:8]=[C:7]2[CH2:6][CH2:5][NH:4][C:1](=[O:3])[CH3:2])=[CH:12][CH:13]=1)(=[O:19])=[O:18]

Participants

5

Procedure

0.8 mmol of the compound obtained in Step B is dissolved in 10 ml of CH2Cl2 and then 1.2 mmol of triethylamine are added. The mixture is cooled with the aid of an ice bath and 1.2 mmol of ammonium hydroxide solution are added dropwise. After stirring for 2 hours, the mixture is evaporated and the residue obtained is recrystallised.

Workup

  1. temperatureThe mixture is cooled with the aid of an ice bath
  2. customthe mixture is evaporated
  3. customthe residue obtained
  4. customis recrystallised

Sources & evidence

ORD record
ord-02eda4db408545648e5b9ef0f79b9ea6
Source dataset
uspto-grants-2007_02
Patent number
US07183318B2

Reaction notes

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