تفاعل #477305

ord-5da196206360430eaaa9852d18008c11

معادلة التفاعل

C=CCCCCN(C)C(=O)C1CC(O)CC1C(=O)NC1(C(=O)OCC)CC1C=C
Compound 1c
C=CCCCCN(C)C(=O)C1CC(O)CC1C(=O)NC1(C(=O)OCC)CC1C=C
1-{[2-(Hex-5-enylmethylcarbamoyl)-4-hydroxycyclopentanecarbonyl]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
title compound
المردود 90.0%
C=CCCCCN(C)C(=O)C1CC(O)CC1C(=O)NC1(C(=O)O)CC1C=C
1-{[2-(Hex-5-enylmethylcarbamoyl)-4-hydroxycyclopentanecarbonyl]amino}-2-vinylcyclopropanecarboxylic acid
المردود 90.0%

المذيبات

ظروف التفاعل

درجة الحرارة
40°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىtransferred to a 20 ml microwave reaction vessel
  2. 2
    أخرىThe reaction vessel was sealed
  3. 3
    أخرىThe reaction was irradiated for 30 min to 130° C
  4. 4
    استخلاصextracted 3 times with EtOAc (20 ml)
  5. 5
    غسيلThe pooled organic layers were washed with brine
  6. 6
    تجفيفdried (MgSO4)
  7. 7
    ترشيحfiltered
  8. 8
    أخرىThe solvent was evaporated in vacuo

الإجراء التجريبي

Compound 1c (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 the title compound (410 mg, 90%). LC/MS >95%, m/z (ESI+)=379(MH+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08383584B2uspto-grants-2013_02