反应 #312615

ord-205a888a3d854f2a95982cedf6ba42b4

反应方程式

O=C(Cl)Oc1ccc([N+](=O)[O-])cc1
4-nitrophenyl chloroformate
c1ccncc1
pyridine
Nc1ccc(N2CCOCC2=O)c(Cl)c1
4-(4-amino-2-chlorophenyl)morpholin-3-one
CC(C)(C)OC(=O)N1CCCN1
tert-butyl pyrazolidine-1-carboxylate
CCN(C(C)C)C(C)C
N-ethyldiisopropylamine
CC(C)(C)OC(=O)N1CCCN1C(=O)Nc1ccc(N2CCOCC2=O)c(Cl)c1
tert-Butyl 2-[3-chloro-4-(3-oxomorpholin-4-yl)phenylcarbamoyl]pyrazolidine-1-carboxylate

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGAfter stirring at RT for 20 h
  2. 2
    其他giving 420 mg (57.3%) of step 1

实验过程

340 mg (1.5 mmol) of 4-(4-amino-2-chlorophenyl)morpholin-3-one are dissolved in 10 ml of dichloromethane (DCM), 302 mg (1.5 mmol) of 4-nitrophenyl chloroformate and 121 μl (1.5 mmol) of pyridine are subsequently added successively, and the mixture is stirred at RT for 1 h. 300.0 mg (0.7 mmol) of tert-butyl pyrazolidine-1-carboxylate and 0.765 mg (4.5 mmol) of N-ethyldiisopropylamine are added to this reaction mixture. After stirring at RT for 20 h, the mixture is subjected to conventional work-up, giving 420 mg (57.3%) of step 1; MS (FAB) m/e=425/427 (M+H)+.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07557102B2uspto-grants-2009_07