Hydrochloric Acid → HCID 69593204, compound

HRID 1825251Notes

Reaction equation

HRID 1825251 reaction equation
[CH2:1]([N:8]1[CH:12]=[CH:11][C:10]([CH2:13][C@@H:14]([NH:18][C@@H:19]([CH2:23][CH:24]([CH3:26])[CH3:25])[C:20]([OH:22])=[O:21])[C:15]([OH:17])=[O:16])=[N:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([C@@H](N[C@@H](CC(C)C)C(O)=O)CC1C=CN(CC2C=C(Cl)C=C(Cl)C=2)N=1)(O)=O.N1C=CC(C(O)=O)=N1.ClC1C=C(C=C(Cl)C=1)CBr.C(Br)C1C=CC=CC=1.ClC1C=C(C=C(Cl)C=1)CN1C=CC(CC2C(OC)=NC(C(C)C)C(OC)=N2)=N1.Cl.C(OC(=O)C(NC(C1C=CN(CC2C=C(Cl)C=C(Cl)C=2)N=1)(C(OC)=O)C)CC(C)C)C1C=CC=CC=1>[OH-].[Na+]>[CH2:1]([N:8]1[CH:12]=[CH:11][C:10]([CH2:13][C@H:14]([NH:18][C@@H:19]([CH2:23][CH:24]([CH3:26])[CH3:25])[C:20]([OH:22])=[O:21])[C:15]([OH:17])=[O:16])=[N:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

10

Reactant 8

HCID 313Hydrochloric Acid2×HCID 7498Benzyl BromideHCID 125839781-(Bromomethyl)-3,5-dichlorobenzeneHCID 58633028HCID 58633028, compoundHCID 69592949HCID 69592949, compoundHCID 86591929HCID 86591929, compoundHCID 131725758HCID 131725758, compoundHCID 178524567HCID 178524567, compound2×

Product 1

HCID 69593204HCID 69593204, compound

Reagents, catalysts & solvents 1

HCID 14798Sodium HydroxideSolvent2×

Procedure

1H NMR (300 MHz, CD3OD) δ 7.60 (d, 1H, J=2.3 Hz); 7.22–7.35 (m, 5H); 6.23 (d, 1H, J=2.4 Hz); 5.31 (s, 2H); 3.86 (dd, 1H, J1=4.7 Hz, J2'7.9 Hz); 3.78 (dd, 1H, J1=J2=6.7 Hz); 3.27–3.30 (m, 1H); 3.17 (dd, 1H, J1=8.1 Hz, J2=15.8 Hz); 1.82–1.91 (m, 1H); 1.68–1.74 (m, 2H); 0.98 (d, 3H, J=4.5 Hz); 0.96 (d, 3H, J=4.5 Hz). Anal. Calc'd. for C19H25N3O4.2/3H2O: % C, 61.44; % H, 7.15; % N, 11.31. Found: % C, 61.00; % H, 6.75; and % N, 11.17. (S,R)-2-[2-(1-benzyl-1H-pyrazol-3-yl)-1-carboxy-ethylamino]-4-methyl pentanoic acid: 1H NMR (300 MHz, CD3OD) δ 7.64 (d, 1H, J=2.4 Hz); 7.22–7.37 (m, 5H); 6.23 (d, 1H, J=2.3 Hz); 5.31 (s, 2H); 3.96–4.00 (m, 1H); 3.77–3.82 (m, 1H); 3.28–3.30 (m, 2H); 1.55–1.80 (m, 3H); 0.86 (d, 3H, J=6.6 Hz); 0.84 (d, 3H, J=6.4 Hz). 52-6a: (R=3,5-diCl-PhCH2) (S,S)-2-{1-carboxy-2-[1-(3,5-dichlorobenzyl)-1H-pyrazol-3-yl]-ethylamino}-4-methyl pentanoic acid. Crude pyrazole 3-carboxylic acid was treated with 3,5-dichlorobenzyl bromide in a manner analogous to the treatment of pyrazole 3-carboxylic acid with benzyl bromide. The same procedures were used to carry the material through to 2-[1-(3,5-dichlorobenzyl)-1H-pyrazol-3ylmethyl]-5-isopropyl-3,6-dimethyoxy-2,5-dihydropyrazine, which was isolated as a single isomer. Hydrolysis with HCl, preparation of the methyl ester, and alkylation of the amine proceeded as described above. 2-{2-[1-[1-(3,5-dichlorobenzyl)-1H-pyrazol-3-yl]-1-methoxycarbonyl-ethylamino}-4-methyl pentanoic acid benzyl ester was treated with NaOH as described above. Purification of the resulting diacid was accomplished by column chromatography (ISCO purification system, C-18 bondisil, H2O to MeOH over 30 min) to give a white powder. This material was dissolved in 1N NaOH solution (aqueous) and then treated with 1 N HCl (aqueous) until pH of 1 was obtained. The resulting precipitate was isolated by filtration to give a white solid (Compound LP). 1H NMR (300 MHz, CD3OD) δ 7.71 (d, 1H, J=2.0 Hz); 7.37 (s, 1H); 7.21 (s, 2H); 6.28 (d, 2H, J=2.4 Hz); 5.30 (s, 2H); 4.05 (dd, 1H, J1=4.9 Hz, J2=7.7 Hz); 3.93 (dd, 1H, J1=J2=6.9 Hz); 3.34 (dd, 1H, J1=4.5 Hz, J2=15.9 Hz); 3.21 (dd, 1H, J1=7.7 Hz, J2=15.9 Hz); 1.85–1.70 (m, 3H); 0.99 (d, 3H, J=2.8 Hz); 0.97 (d, 3H, J=2.4 Hz). Anal. Calc'd for C19H23Cl2N3O4.H2O: % C, 51.13; % H, 5.65; % Cl, 15.89; % N, 9.41. Found: % C, 51.41; % H, 5.24; % Cl, 16.24; and % N, 9.42.

Workup

  1. customwhich was isolated as a single isomer
  2. customHydrolysis
  3. customPurification of the resulting diacid
  4. customwas accomplished by column chromatography (ISCO purification system, C-18 bondisil, H2O to MeOH over 30 min)
  5. customto give a white powder
  6. customwas obtained
  7. customThe resulting precipitate was isolated by filtration
  8. customto give a white solid (Compound LP)

Sources & evidence

ORD record
ord-6dd743c5a21145bea2eef53c4d1266fc
Source dataset
uspto-grants-2006_05
Patent number
US07045532B2

Reaction notes

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