Acetic Acid → 3-(2-{6-methyl-2-oxo-3-[(5,6,7,8-tetrahydro-[1,8]naphthyridin-2-ylmethyl)-amino]-2H-pyridin-1-yl}-acetylamino)-3(S)-pyridin-3-yl-propionic acid ethyl ester

HRID 1602666Notes

Reaction equation

HRID 1602666 reaction equation
[CH2:1]([O:3][C:4](=[O:26])[CH2:5][C@H:6]([NH:13][C:14](=[O:25])[CH2:15][N:16]1[C:21]([CH3:22])=[CH:20][CH:19]=[C:18]([NH2:23])[C:17]1=[O:24])[C:7]1[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=1)[CH3:2].[N:27]1[C:36]2[NH:35][CH2:34][CH2:33][CH2:32][C:31]=2[CH:30]=[CH:29][C:28]=1[CH:37]=O.CC(O)=O.[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+]>C(Cl)(Cl)Cl.CO>[CH2:1]([O:3][C:4](=[O:26])[CH2:5][C@H:6]([NH:13][C:14](=[O:25])[CH2:15][N:16]1[C:21]([CH3:22])=[CH:20][CH:19]=[C:18]([NH:23][CH2:37][C:28]2[CH:29]=[CH:30][C:31]3[CH2:32][CH2:33][CH2:34][NH:35][C:36]=3[N:27]=2)[C:17]1=[O:24])[C:7]1[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=1)[CH3:2]

Participants

7

Procedure

##STR55## To a solution of the amine 16-6 (155 mg, 0.433 mmol), the aldehyde 14-3 (70 mg, 0.433 mmol) in CH2ClCH2Cl was added crushed 4A seives, AcOH (20 μL) and then NaB(OAc)3H (184 mg, 0.866 mmol). After stirring for 48 hours, the mixture was filtered through celite, poured into EtOAc and washed with saturated NaHCO3 then brine. The dried (MgSO4) solution was concentrated in vacuo to give a foam type solid. Column chromatography (5%MeOH in CHCl3) afforded the title compound 16-7 as a foam type solid.

Workup

  1. filtrationthe mixture was filtered through celite
  2. additionpoured into EtOAc
  3. washwashed with saturated NaHCO3
  4. dry with materialThe dried (MgSO4) solution
  5. concentrationwas concentrated in vacuo
  6. customto give a foam type solid

Sources & evidence

ORD record
ord-4ba850b499bc4923b2c6b5b8d8c7827c
Source dataset
uspto-grants-1999_11
Patent number
US05981546

Reaction notes

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