反应 #657301

ord-0384043e43ac4bad8eb339fcffc9b52d

反应方程式

C=CCCCCN(C)C(=O)C1CC(O)CC1C(=O)NC1(C(=O)OCC)CC1C=C
Compound 6
C=CCCCCN(C)C(=O)C1CC(O)CC1C(=O)NC1(C(=O)OCC)CC1C=C
1-{[2-(Hex-5-enylmethylcarbamoyl)-4-hydroxycyclopentane carbonyl]amino}-2-vinylcyclopropane carboxylic acid ethyl ester
[Li+].[OH-]
LiOH
Cl
HCl
C=CCCCCN(C)C(=O)C1CC(O)CC1C(=O)NC1(C(=O)O)CC1C=C
compound 7
收率 90.0%
C=CCCCCN(C)C(=O)C1CC(O)CC1C(=O)NC1(C(=O)O)CC1C=C
1-{[2-(Hex-5-enylmethylcarbamoyl)-4-hydroxycyclopentane-carbonyl]amino}-2-vinylcyclopropanecarboxylic acid
收率 90.0%

溶剂

反应条件

温度
40°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他transferred to a 20 mL microwave reaction vessel
  2. 2
    其他The reaction vessel was sealed
  3. 3
    其他The reaction was irradiated for 30 min to 130° C
  4. 4
    萃取extracted 3 times with EtOAc (20 mL)
  5. 5
    洗涤The pooled organic layers were washed with brine
  6. 6
    干燥dried (MgSO4)
  7. 7
    过滤filtered
  8. 8
    其他The solvent was evaporated in vacuo

实验过程

Compound 6 (493 mg, 1.21 mmol) was dissolved in DMF (1 mL) and transferred to a 20 mL microwave reaction vessel. Then, aqueous LiOH (2 M, 10.5 mL) and a stirbar were added. The reaction vessel was sealed and the immiscible slurry was shaken vigorously before insertion in the microwave cavity. The reaction was irradiated for 30 min to 130° C. The reaction mixture was cooled to 40° C. and the clear solution acidified to pH 2 with aqueous HCl (1 M, 24 mL) and extracted 3 times with EtOAc (20 mL). The pooled organic layers were washed with brine, dried (MgSO4) and filtered. The solvent was evaporated in vacuo to afford compound 7 (410 mg, 90%). LC/MS (Method A): tR=2.46 min, >95%, m/z (ESI+)=379 (MH+).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09023808B2uspto-grants-2015_05