Hydrochloric Acid → HCID 18511133, compound

HRID 1371219Notes

Reaction equation

HRID 1371219 reaction equation
[CH3:1][C:2]1[NH:3][C:4]2[C:5]([N:14]=[C:15]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH:16]=2)=[C:6]([N:8]2CCOCC2)[N:7]=1.[Cl:23][CH:24]([CH:28]1[O:32][CH2:31][CH2:30][O:29]1)[CH2:25][CH2:26][CH3:27].N(CC)(C(C)C)C(C)C.Cl>C1(C)C=CC=CC=1.CN(C=O)C.C(Cl)Cl.CCOC(C)=O>[ClH:23].[O:29]1[CH2:30][CH2:31][O:32][CH:28]1[CH2:24][CH2:25][CH2:26][CH2:27][N:14]1[C:5]2[C:6]([NH2:8])=[N:7][C:2]([CH3:1])=[N:3][C:4]=2[CH:16]=[C:15]1[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

Participants

7

Reactant 4

HCID 313Hydrochloric AcidHCID 81531DiisopropylethylamineHCID 18511167HCID 18511167, compoundHCID 178433100HCID 178433100, compound

Product 1

HCID 18511133HCID 18511133, compoundYield 23%

Reagents, catalysts & solvents 2

HCID 21226138Dichloromethane ethylacetateSolventHCID 21735183Dimethylformamide tolueneSolvent

Procedure

A solution of 2-methyl-4-amino-6-phenylpyrrolo[3,2-d]pyrimidine (Example 22) (0.079 g, 0.35 mmol), 2-(1-chlorobutyl)-1,3-dioxolane (Fluka Chemika) (0.14 g, 0.85 mmol), and iso-Pr2NEt (0.3 mL, 1.7 mmol) in toluene/DMF (2.5:1.0 mL) was heated at reflux for 6 days. The mixture was allowed to cool to room temperature and purified by flash chromatography on silica gel with 5% NH3 (2N in MeOH) 5% MeOH in CH2Cl2 to afford the product. The product was dissolved in CH2Cl2/EtOAc (1:1) and the solution was treated with a 2 M ethereal HCl (2 mL). The resulting slurry was filtered, and the solid was washed with hot EtOAc (3×) to give a yellow solid (29 mg, 23%). 1H NMR (DMSO-d6; 400 MHz): d 1.53 (m, 2), 1.64 (m, 2), 1.84 (m, 2), 2.68 (s, 3), 3.86 (m, 2), 4.32 (br t, 2), 4.80 (t, 1), 7.34 (s, 1), 7.48-7.58 (m, 3), 8.11 (d, 2), 8.89 (s, 1), 9.17 (s, 1), 13.90 (s, 1). MS m/z: 353 (M+1). Anal. Calcd for C20H24N4O2.2HCl: C, 56.47; H, 6.16; N, 13.18. Found: C, 56.36; H, 6.08; N, 13.21.

Workup

  1. temperatureat reflux for 6 days
  2. custompurified by flash chromatography on silica gel with 5% NH3 (2N in MeOH) 5% MeOH in CH2Cl2
  3. customto afford the product
  4. filtrationThe resulting slurry was filtered
  5. washthe solid was washed with hot EtOAc (3×)

Sources & evidence

ORD record
ord-741d132bf26a45b182681e1bf86a3e4f
Source dataset
uspto-grants-2003_06
Patent number
US06583154B1

Reaction notes

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