Hydrochloric Acid → HCID 178466729, compound

HRID 510954Notes

Reaction equation

HRID 510954 reaction equation
[Cl:1][C:2]1[C:3]([CH3:37])=[C:4]([CH:23]2[CH2:26][N:25](C(OCC3C=CC=CC=3)=O)[CH2:24]2)[C:5]([O:20][CH2:21][CH3:22])=[C:6]([CH:8]([NH:10][C:11]2[N:19]=[CH:18][N:17]=[C:16]3[C:12]=2[N:13]=[CH:14][NH:15]3)[CH3:9])[CH:7]=1.Cl.O>CO.[Pd]>[NH:25]1[CH2:26][CH:23]([C:4]2[C:5]([O:20][CH2:21][CH3:22])=[C:6]([CH:8]([NH:10][C:11]3[N:19]=[CH:18][N:17]=[C:16]4[C:12]=3[N:13]=[CH:14][NH:15]4)[CH3:9])[CH:7]=[C:2]([Cl:1])[C:3]=2[CH3:37])[CH2:24]1

Participants

6

Reactant 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 178466731HCID 178466731, compound

Product 1

HCID 178466729HCID 178466729, compound

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent

Procedure

Benzyl 3-{3-chloro-6-ethoxy-2-methyl-5-[1-(9H-purin-6-ylamino)ethyl]phenyl}azetidine-1-carboxylate (83 mg, 0.16 mmol) and 5% palladium (74 mg) was combined in methanol (5 mL), to which was added 0.25 M HCl in water (1.6 mL, 0.40 mmol). The suspension was hydrogenated under balloon pressure of H2 at room temperature overnight. The suspension was filtered and concentrated to give N-[1-(3-azetidin-3-yl-5-chloro-2-ethoxy-4-methylphenyl)ethyl]-9H-purin-6-amine. LCMS calculated for C19H24ClN6O (M+H)+: m/z=387.2. found: 387.1. The azetidine made above was combined with DIPEA (0.1 mL, 0.6 mmol) in methanol (0.5 mL)/acetonitrile (0.5 mL)/THF (0.5 mL), followed by the addition of 37% formaldehyde (0.1 mL, 2 mmol). The mixture was stirred at room temperature for 10 min before the addition of sodium triacetoxyborohydride (0.17 g, 0.80 mmol). The reaction mixture was stirred at room temperature overnight, then diluted with MeOH and purified on RP-HPLC (XBridge C18 Column, eluting with a gradient of acetonitrile in water with 0.2% ammonium hydroxide, at flow rate of 30 mL/min) to give the desired product. LCMS calculated for C20H26ClN6O (M+H)+: m/z=401.2. found: 401.1.

Workup

  1. filtrationThe suspension was filtered
  2. concentrationconcentrated

Sources & evidence

ORD record
ord-58e984b3741447b2a9cf4cd056517093
Source dataset
uspto-grants-2015_08
Patent number
US09096600B2

Reaction notes

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