반응 #44483

ord-98f233ee8b804324a16424ad2de60716

반응 방정식

[NH4+].[OH-]
NH4OH
O=C(O)C(F)(F)F
Trifluoroacetic acid
CC(C)(C)OC(=O)N1CCCC(N2CC(COc3ccc(C#N)cn3)C(C)(C)C2=O)CC1
solution
CC(C)(C)OC(=O)N1CCCC(N2CC(COc3ccc(C#N)cn3)C(C)(C)C2=O)CC1
4-[4-(5-cyano-pyridin-2-yloxymethyl)-3,3-dimethyl-2-oxo-pyrrolidin-1-yl]-azepane-1-carboxylic acid tert-butyl ester
O=C(OC(Cl)(Cl)Cl)OC(Cl)(Cl)Cl
Triphosgene
CC1(C)C(=O)N(C2CCCN(C(N)=O)CC2)CC1COc1ccc(C#N)cn1
title compound
CC1(C)C(=O)N(C2CCCN(C(N)=O)CC2)CC1COc1ccc(C#N)cn1
4-(4-{[(5-cyanopyridin-2-yl)oxy]methyl}-3,3-dimethyl-2-oxopyrrolidin-1-yl)azepane-1-carboxamide

반응 조건

온도
-78°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The solvent was evaporated in vacuo
  2. 2
    workup.STIRRINGstirred for one hour
  3. 3
    workup.ADDITIONwas added
  4. 4
    workup.STIRRINGstirred at room temperature for one hour
  5. 5
    추출The product was extracted with dichloromethane
  6. 6
    건조dried with MgSO4
  7. 7
    여과filtered
  8. 8
    기타evaporated in vacuo
  9. 9
    기타The crude reaction mixture
  10. 10
    기타was purified by preparative reverse phase HPLC on a Waters Symmetry C8 column (25 mm×100 mm, 7 um particle size)

실험 절차

Trifluoroacetic acid (0.75 mL) was added to a solution of Example 2F (0.108 g, 0.24 mmoles) in dichloromethane (0.75 mL) and stirred for one hour. The solvent was evaporated in vacuo. The residue was taken in dichloromethane (1.5 mL) and cooled to −78° C. Triphosgene (24 mg, 0.08 mmoles) was added and stirred for one hour. To the reaction, NH4OH (1 mL) was added and stirred at room temperature for one hour. The product was extracted with dichloromethane, dried with MgSO4, filtered, and evaporated in vacuo. The crude reaction mixture was purified by preparative reverse phase HPLC on a Waters Symmetry C8 column (25 mm×100 mm, 7 um particle size) using a gradient of 20% to 100% acetonitrile:water (0.1% trifluoroacetic acid) over eighteen minutes at a flow rate of 40 mL/minute to provide the title compound. 1H NMR (300 MHz, CDCl3) δ ppm 8.48 (dd, J=2.33, 0.64 Hz, 1H), 7.80 (dd, J=8.66, 2.33 Hz, 1H), 6.82 (dd, J=8.66, 0.78 Hz, 1H), 5.81 (b,r, 2H), 4.50 (dd, J=10.87, 6.04 Hz, 1H), 4.36 (dd, J=10.86, 8.24 Hz, 1H), 4.03-4.19 (m, 1H), 3.16 (m, 4H), 3.46 (dd, J=9.85, 7.64 Hz, 1H), 3.08 (dd, J=9.87, 7.94 Hz, 1H), 2.45 (qd, J=7.94, 6.01 Hz, 1H), 1.43-1.82 (m, 6H), 1.24 (s, 3H), 1.06 (s, 3H). MS (APCI+) m/z 386.2 (M+H)+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07737137B2uspto-grants-2010_06