1-Pentanol → HCID 178447150, compound

HRID 448618Notes

Reaction equation

HRID 448618 reaction equation
[NH2:1][C@H:2]([CH2:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[CH:14][CH:13]=1)[CH2:3][C@:4]([CH2:9][OH:10])([CH3:8])[C:5]([OH:7])=[O:6].CC#N.O1CCOCC1.[CH2:33](O)[CH2:34][CH2:35][CH2:36][CH3:37].[NH:39]1[CH:43]=[C:42]([C:44](O)=[O:45])[N:41]=[N:40]1.CCN(C(C)C)C(C)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F>Cl.CN(C=O)C>[CH2:33]([O:6][C:5](=[O:7])[C@@:4]([CH2:9][OH:10])([CH3:8])[CH2:3][C@H:2]([NH:1][C:44]([C:42]1[NH:41][N:40]=[N:39][CH:43]=1)=[O:45])[CH2:11][C:12]1[CH:13]=[CH:14][C:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[CH:16][CH:17]=1)[CH2:34][CH2:35][CH2:36][CH3:37]

Participants

10

Reactant 7

HCID 62761-PentanolHCID 6342AcetonitrileHCID 312751,4-DioxaneHCID 81531Diisopropylethylamine2×HCID 1401204-Carboxy-1,2,3-triazoleHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 68181056(2S,4R)-4-Amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methylpentanoic acid

Product 1

HCID 178447150HCID 178447150, compound

Reagents, catalysts & solvents 2

HCID 313Hydrochloric AcidSolventHCID 6228DimethylformamideSolvent2×

Procedure

(2S,4R)-4-Amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid (76 mg, 242 μmol) in MeCN (0.4 mL, 8 mmol) and 4 M HCl in 1,4-dioxane (242 μL, 969 μmol) was combined with pentan-1-ol (0.5 mL) at 60° C. The resulting mixture was stirred until solid precipitation was observed (˜30 minutes). The solvent was evaporated under vacuum and the solids were azeotroped in toluene and dried under vacuum. 1,2,3-Triazole-4-carboxylic acid (0.0274 g, 0.242 mmol), DIPEA (169 μL, 969 μmol) and HATU (92 mg, 242 μmol) were combined in DMF (0.2 mL) and stirred for 5 minutes at room temperature. This was then combined with the dried solids, predissolved in DMF (0.2 mL) and DIPEA (0.5 eq.). The resulting mixture was stirred for 15 minutes and the reaction was quenched with AcOH. The product was purified by preparative HPLC and lyophilized to yield the title compound (30 mg; purity 95%). MS m/z [M+H]+ calc'd for C27H34N4O4, 479.26. found 479.4.

Workup

  1. custom(˜30 minutes)
  2. customThe solvent was evaporated under vacuum
  3. customthe solids were azeotroped in toluene
  4. customdried under vacuum
  5. stirringstirred for 5 minutes at room temperature
  6. stirringThe resulting mixture was stirred for 15 minutes
  7. customthe reaction was quenched with AcOH
  8. customThe product was purified by preparative HPLC

Sources & evidence

ORD record
ord-9ca8cb9c33da4ee2bddd31a21c5ac750
Source dataset
uspto-grants-2013_07
Patent number
US08481044B2

Reaction notes

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