تفاعل #2358491

ord-60203926175545d8aa4c8184c44eb8db

معادلة التفاعل

O
water
CC(C)(C)OC(=O)N1C(=O)CC2CC=CC21
tert-butyl 2-oxo-3,3a,4,6a-tetrahydrocyclopenta[b]pyrrole-1-carboxylate
CN(C)C(OC(C)(C)C)N(C)C
tert-butoxybis(dimethylamino)methane
CN(C)C=C1C(=O)N(C(=O)OC(C)(C)C)C2C=CCC12
desired compound
المردود 58.0%
CN(C)C=C1C(=O)N(C(=O)OC(C)(C)C)C2C=CCC12
tert-butyl-3-(dimethylaminomethylene)-2-oxo-4,6a-dihydro-3aH-cyclopenta[b]pyrrole-1-carboxylate
المردود 58.0%

المذيبات

ظروف التفاعل

درجة الحرارة
110°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةIt was then cooled to room temperature
  2. 2
    استخلاصextracted 3 times
  3. 3
    غسيلThe combined organic layers were washed with brine
  4. 4
    أخرىdried
  5. 5
    تركيزconcentrated
  6. 6
    أخرىpurified by flash chromatography (5% MeOH in CH2Cl2)

الإجراء التجريبي

To a solution of tert-butyl 2-oxo-3,3a,4,6a-tetrahydrocyclopenta[b]pyrrole-1-carboxylate IV-1 (500 mg, 2.23 mmol) in toluene (11 mL) was added tert-butoxybis(dimethylamino)methane (1.39 mL, 6.71 mmol) The solution was heated for 2 h at 110° C. It was then cooled to room temperature, poured into water (20 mL), diluted with ethyl acetate (20 mL), and extracted 3 times. The combined organic layers were washed with brine, dried, concentrated and purified by flash chromatography (5% MeOH in CH2Cl2) giving the desired compound as a brown solid (367 mg, 58%); 1H NMR (400 MHz, CDCl3) 7.12 (1H, s), 5.99 (1H, m), 5.85 (1H, m), 4.91 (1H, d), 3.70 (1H, m), 3.03 (6H, s), 2.79 (1H, m), 2.40 (1H, dd), 1.54 (9H, s); LCMS (Method A): 0.83 min; ES+279 (M+H+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09119398B2uspto-grants-2015_09