Processes for preparing a diazabicyclooctane compound
A process for preparing a diazabicyclooctane compound represented by the following formula (I): wherein A represents RcO—; B represents NH or NC 1-6 alkyl; C represents a benzyl group; Rc represents a C 1-6 alkyl group; A is substituted with one substituent Fn1, wherein Fn1 represents an azetidine group; the process including: (a) silylating the compound represented by the following formula (IV-c): wherein in the formula (IV-c), OBn represents benzyloxy, and (b) carrying out an intramolecular urea formation reaction.
1. A process for preparing (2S,5R)-N-(2-aminoethoxy)-7-oxo-6-(sulfooxy)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide represented by the following formula (III-059):
which comprises:
removing the benzyl of the benzyloxy at the 6-position of a compound represented by the following formula (IIa-Boc-059):
wherein in the formula (IIa-Boc-059), Boc represents tert-butoxycarbonyl, and OBn represents benzyloxy,
in the presence of palladium-carbon under a hydrogen atmosphere to prepare a compound represented by the following formula (IIb-Boc-059):
wherein in the formula (IIb-Boc-059), Boc represents tert-butoxycarbonyl, sulfating the hydroxyl group at the 6-position of the formula (IIb-Boc-059) with a sulfur trioxide-pyridine complex in the presence of pyridine, 2-picoline or 2,6-lutidine to prepare a compound represented by the following formula (III-Boc-059):
wherein in the formula (III-Boc-059), Boc represents tert-butoxycarbonyl, and M represents H, pyridinium, sodium or tetrabutylammonium, and deprotecting the tert-butoxycarbonyl group with an acid selected from the group consisting of hydrochloric acid, sulfuric acid, methanesulfonic acid, trifluoroacetic acid and tetrafluoroboric acid.
2. The process of claim 1 , wherein the sulfating of the hydroxyl group at the 6-position of the formula (IIb-Boc-059) with the sulfur trioxide-pyridine complex is performed in the presence of 2-picoline or 2,6-lutidine.
3. The process of claim 1 , wherein in the formula (III-Boc-059), M represents pyridinium, sodium or tetrabutylammonium.