Triethylamine → HCID 9881916, compound

HRID 428170Notes

Reaction equation

HRID 428170 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[CH:15]=[CH:14][C:13]3[O:12][CH2:11][CH:10](C(O)=O)[CH2:9][C:8]=3[C:7]=2[CH:19]=1.[CH2:20]([N:22](CC)CC)[CH3:21].ClC(OCC)=[O:29].[N-]=[N+]=[N-].[Na+]>CC(C)=O.O>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[CH:15]=[CH:14][C:13]3[O:12][CH2:11][CH:10]([NH:22][C:20](=[O:29])[CH3:21])[CH2:9][C:8]=3[C:7]=2[CH:19]=1

Participants

7

Procedure

After dissolving the acid obtained in Step B (50 mg:0.19 mmol) in acetone (2 ml) under an inert atmosphere, distilled triethylamine (0.07 ml:0.52 mmol:2.7 eq.) and also distilled ethyl chloroformate (0.06 ml:0.68 mmol:3.5 eq.) are slowly introduced in succession at 0° C. After 30 minutes of stirring, sodium azide (57 mg:0.87 mmol:4.5 eq.), dissolved in 1 ml of water, is added. After a similar amount of time has passed, the reaction medium is extracted with dichloromethane. The resulting organic phase is concentrated, taken up in I ml of toluene and heated at reflux for 30 minutes. While in the hot state, glacial acetic acid (1 ml) is then introduced; the heating is then continued for 1 hour 30 minutes. At ambient temperature, the products are extracted with ethyl acetate and then purified on a flash silica column CHCl3/AcOEt 7/3. The title compound is washed with diethyl ether.

Workup

  1. additionare slowly introduced in succession at 0° C
  2. additionis added
  3. extractionthe reaction medium is extracted with dichloromethane
  4. concentrationThe resulting organic phase is concentrated
  5. temperatureheated
  6. temperatureat reflux for 30 minutes
  7. additionWhile in the hot state, glacial acetic acid (1 ml) is then introduced
  8. waitthe heating is then continued for 1 hour 30 minutes
  9. extractionAt ambient temperature, the products are extracted with ethyl acetate
  10. custompurified on a flash silica column CHCl3/AcOEt 7/3
  11. washThe title compound is washed with diethyl ether

Sources & evidence

ORD record
ord-08ebad98c20f4cf5b25db6b4e94f023e
Source dataset
uspto-grants-2001_11
Patent number
US06313160B1

Reaction notes

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