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Acetic Acid → 4-(((R)-2-Hydroxy-2-(8-hydroxy-2-oxo-1,2-dihydroquinolin-5-yl)ethyl)-amino)butyl 1-(4-((3-((S)-phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)methyl)-phenoxy)methyl)benzoyl)piperidine-4-carboxylate

HRID 874813
Notes
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Reaction equation

HRID 874813 reaction equation
Cl.[NH2:2][CH2:3][C@@H:4]([C:6]1[CH:15]=[CH:14][C:13]([OH:16])=[C:12]2[C:7]=1[CH:8]=[CH:9][C:10](=[O:17])[NH:11]2)[OH:5].C(N(CC)CC)C.[C:25]1([C@H:31]([NH:62][C:63]([O:65][C@@H:66]2[CH:71]3[CH2:72][CH2:73][N:68]([CH2:69][CH2:70]3)[CH2:67]2)=[O:64])[C:32]2[CH:33]=[C:34]([CH:59]=[CH:60][CH:61]=2)[O:35][CH2:36][C:37]2[CH:58]=[CH:57][C:40]([C:41]([N:43]3[CH2:48][CH2:47][CH:46]([C:49]([O:51][CH2:52][CH2:53][CH2:54][CH:55]=O)=[O:50])[CH2:45][CH2:44]3)=[O:42])=[CH:39][CH:38]=2)[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(O)(=O)C>CO>[C:25]1([C@H:31]([NH:62][C:63]([O:65][C@@H:66]2[CH:71]3[CH2:70][CH2:69][N:68]([CH2:73][CH2:72]3)[CH2:67]2)=[O:64])[C:32]2[CH:33]=[C:34]([CH:59]=[CH:60][CH:61]=2)[O:35][CH2:36][C:37]2[CH:58]=[CH:57][C:40]([C:41]([N:43]3[CH2:44][CH2:45][CH:46]([C:49]([O:51][CH2:52][CH2:53][CH2:54][CH2:55][NH:2][CH2:3][C@H:4]([OH:5])[C:6]4[CH:15]=[CH:14][C:13]([OH:16])=[C:12]5[C:7]=4[CH:8]=[CH:9][C:10](=[O:17])[NH:11]5)=[O:50])[CH2:47][CH2:48]3)=[O:42])=[CH:39][CH:38]=2)[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 5

HCID 176Acetic AcidHCID 8471TriethylamineHCID 5049666Sodium triacetoxyborohydrideHCID 71093241(R)-5-(2-Amino-1-hydroxyethyl)-8-hydroxyquinolin-2(1H)-one hydrochlorideHCID 867223044-Oxobutyl 1-(4-((3-((S)-phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)-methyl)phenoxy)methyl)benzoyl)piperidine-4-carboxylate

Product 1

HCID 74762660
4-(((R)-2-Hydroxy-2-(8-hydroxy-2-oxo-1,2-dihydroquinolin-5-yl)ethyl)-amino)butyl 1-(4-((3-((S)-phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)methyl)-phenoxy)methyl)benzoyl)piperidine-4-carboxylate
Yield 16.5%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent2×

Procedure

To a suspension of (R)-5-(2-amino-1-hydroxyethyl)-8-hydroxyquinolin-2(1H)-one hydrochloride (0.136 g, 0.53 mmol) in methanol (3.5 mL) was added triethylamine (0.148 mL, 1.06 mmol). The mixture was stirred for 10 minutes and then a solution of 4-oxobutyl 1-(4-((3-((S)-phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)methyl)-phenoxy)methyl)benzoyl)piperidine-4-carboxylate (0.337 g, 0.50 mmol) in methanol (3.4 mL) was added. The mixture was stirred at RT for 1 hour. Sodium triacetoxyborohydride (0.267 g, 1.26 mmol) followed by acetic acid (0.121 mL, 2.12 mmol) was added and the reaction continued for a further 18 hours. The reaction mixture was quenched with water and evaporated at reduced pressure. The residue dissolved in iso-butanol and washed with water. The organic phase was evaporated at reduced pressure and the crude material was purified by reverse phase preparative HPLC to afford the title compound (0.072 g, 16%).

Workup

  1. stirringThe mixture was stirred at RT for 1 hour
  2. additionwas added
  3. waitthe reaction continued for a further 18 hours
  4. customThe reaction mixture was quenched with water
  5. customevaporated at reduced pressure
  6. dissolutionThe residue dissolved in iso-butanol
  7. washwashed with water
  8. customThe organic phase was evaporated at reduced pressure
  9. customthe crude material was purified by reverse phase preparative HPLC

Sources & evidence

ORD record
ord-00180ee9b5044d91a8cf5380d2e174f1
Source dataset
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08980913B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes