Reaction #657341

ord-6a778ac198034c638c9e0eb4f50d9896

Reaction equation

[Li+].[OH-]
LiOH
COC(=O)c1ccc2c(c1)NC1NC(=O)N(C3CCN(CCCNC(=O)OC(C)(C)C)CC3)C=C1O2
3-[1-(3-tert-Butoxycarbonylamino-propyl)-piperidin-4-yl]-2-oxo-2,3,9,9a-tetrahydro-1H-10-oxa-1,3,9-triaza-anthracene-7-carboxylic acid methyl ester
CC(C)(C)OC(=O)NCCCN1CCC(n2cc3c(nc2=O)Nc2cc(C(=O)O)ccc2O3)CC1
3-[1-(3-tert-Butoxycarbonylamino-propyl)-piperidin-4-yl]-2-oxo-2,9-dihydro-3H-10-oxa-1,3,9-triaza-anthracene-7-carboxylic acid
Yield 56.0%

Solvents

Conditions

Temperature
50°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.WAITleft
  2. 2
    TemperatureThe reaction solution was cooled to RT
  3. 3
    Extractionextracted with EtOAc
  4. 4
    Otherthe desired product was precipitated
  5. 5
    Filtrationfiltered

Procedure

1M of LiOH aqueous solution (4.5 mL, 3 equiv) and 3-[1-(3-tert-Butoxycarbonylamino-propyl)-piperidin-4-yl]-2-oxo-2,3,9,9a-tetrahydro-1H-10-oxa-1,3,9-triaza-anthracene-7-carboxylic acid methyl ester (5, 760 mg, 1.52 mmol, 1.0 equiv) was added to THF (5 mL), warmed up to 50° C. and stirred until LCMS showed no starting material left. The reaction solution was cooled to RT and extracted with EtOAc. The aqueous layer was acidified to pH 2 and the desired product was precipitated and filtered to yield 3-[1-(3-tert-Butoxycarbonylamino-propyl)-piperidin-4-yl]-2-oxo-2,9-dihydro-3H-10-oxa-1,3,9-triaza-anthracene-7-carboxylic acid (412 mg, 738 mg theoretical, 56%) as a light brown solid. For 6: C24H31N5O6, LCMS (EI) m/e 486(M++H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09023843B2uspto-grants-2015_05