Реакция #58515

ord-c2356eab904a48a39d1543985db7713a

Уравнение реакции

COC(=O)c1cc2c(s1)C1CN(Cc3ccccc3)CC1C2
product
COC(=O)c1cc2c(s1)C1CN(Cc3ccccc3)CC1C2
2-Benzyl-1,2,3,3a,7,7a-hexahydro-4-thia-2-aza-cyclopenta[α]pentalene-5-carboxylic acid methyl ester
O=C([O-])[O-].[K+].[K+]
K2CO3
CC(Cl)OC(=O)Cl
ACE-Cl
COC(=O)c1cc2c(s1)C1CNCC1C2
titled compound
COC(=O)c1cc2c(s1)C1CNCC1C2
1,2,3,3a,7,7a-Hexahydro-4-thia-2-aza-cyclopenta[α]pentalene-5-carboxylic acid methyl ester

Растворители

Условия реакции

Температура
80°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураThe reaction was cooled to room temperature
  2. 2
    Фильтрацияfiltered
  3. 3
    Концентрированиеconcentrated in vacuo
  4. 4
    workup.DISSOLUTIONThe crude oil was dissolved in anhydrous MeOH (2.5 ml)
  5. 5
    workup.STIRRINGstirred at room temperature for 3 hours
  6. 6
    ДругоеThe solvent was evaporated
  7. 7
    Другоеthe product triturated with anhydrous ether
  8. 8
    Другоеto give a white solid, which
  9. 9
    Фильтрацияwas filtered

Методика

To a solution of the product from step b) (100 mg, 0.32 mmol) in DCE (1.6 ml) was added powdered K2CO3 (176 mg, 1.28 mmol) and ACE-Cl (183 mg, 1.28 mmol). The reaction mixture was heated to 80° C. and stirred for 18 hours. The reaction was cooled to room temperature, filtered, and concentrated in vacuo. The crude oil was dissolved in anhydrous MeOH (2.5 ml) and stirred at room temperature for 3 hours. The solvent was evaporated and the product triturated with anhydrous ether to give a white solid, which was filtered to give the titled compound as its hydrochloride salt: (42.3 mg, 51%), 1H NMR (300 MHz, DMSO, ppm) 2.68 (br d, J=16 Hz, 1H), 2.98-3.06 (m, 2H), 3.19-3.28 (m, 1H), 3.35-3.50 (m, 2H), 3.52-3.62 (m, 1H), 3.80 (s, 3H), 4.00-4.11 (m, 1H), 7.56 (s, 1H), 9.05 (br s, 1H), 9.31 (br s, 1H). MS calculated for C11H13NO2S+H 224, observed 224.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07423056B2uspto-grants-2008_09