반응 #2254197

ord-a18da48203c34bd39d301fa12ad72b25

반응 방정식

Cc1ccc(-c2cc(C(F)(F)F)nn2-c2ccc(S(=O)(=O)NC(=O)[C@H](CCCNC(=NS(=O)(=O)c3c(C)c(C)c4c(c3C)CC(C)(C)O4)NOC(C)(C)C)NC(=O)OCC3c4ccccc4-c4ccccc43)cc2)cc1
Compound ( 15a )
Cc1ccc(-c2cc(C(F)(F)F)nn2-c2ccc(S(=O)(=O)NC(=O)[C@H](CCCNC(=NS(=O)(=O)c3c(C)c(C)c4c(c3C)CC(C)(C)O4)NOC(C)(C)C)NC(=O)OCC3c4ccccc4-c4ccccc43)cc2)cc1
(S)-(9H-Fluoren-9-yl)methyl (5-(3-(tert-butoxy)-2-((2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran-5-yl)sulfonyl)guanidino)-1-oxo-1-(4-(5-(p-tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)phenylsulfonamido)pentan-2-yl)carbamate
C1CCNCC1
piperidine
Cc1ccc(-c2cc(C(F)(F)F)nn2-c2ccc(S(=O)(=O)NC(=O)[C@@H](N)CCCNC(N)=NO)cc2)cc1
title compound
Cc1ccc(-c2cc(C(F)(F)F)nn2-c2ccc(S(=O)(=O)NC(=O)[C@@H](N)CCCNC(N)=NO)cc2)cc1
(S)-2-Amino-5-(2-hydroxyguanidino)-N-((4-(5-(p-tolyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)phenyl)sulfonyl)pentanamide

반응 조건

온도
25°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타to remove the Fmoc protecting group
  2. 2
    기타The residue is purified by reverse phase chromatography (acetonitrile/water with 0.05% trifluoroacetic acid)
  3. 3
    workup.DISSOLUTIONdissolved in 95% trifluoroacetic acid-methylene chloride (0.1 M)
  4. 4
    농축concentrated under reduced pressure
  5. 5
    기타The residue is purified by reverse phase chromatography (acetonitrile/water with 0.05% trifluoroacetic acid)

실험 절차

Compound (15a) is treated with 20-50% piperidine in N,N-dimethylformamide (0.1 M) to remove the Fmoc protecting group. The residue is purified by reverse phase chromatography (acetonitrile/water with 0.05% trifluoroacetic acid) and then dissolved in 95% trifluoroacetic acid-methylene chloride (0.1 M). The mixture is stirred at 25° C. for 6 h and then concentrated under reduced pressure. The residue is purified by reverse phase chromatography (acetonitrile/water with 0.05% trifluoroacetic acid) to provide the title compound.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09044464B2uspto-grants-2015_06