Thionyl Chloride → (6-Methoxy-pyridin-3-ylmethyl)-[6-(4-chloromethyl-phenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-amine

HRID 133048Notes

Reaction equation

HRID 133048 reaction equation
[CH3:1][O:2][C:3]1[N:8]=[CH:7][C:6]([CH2:9][NH:10][C:11]2[C:12]3[CH:19]=[C:18]([C:20]4[CH:25]=[CH:24][C:23]([CH2:26]O)=[CH:22][CH:21]=4)[NH:17][C:13]=3[N:14]=[CH:15][N:16]=2)=[CH:5][CH:4]=1.O=S(Cl)[Cl:30]>C(#N)C.O1CCOCC1.CCOC(C)=O>[CH3:1][O:2][C:3]1[N:8]=[CH:7][C:6]([CH2:9][NH:10][C:11]2[C:12]3[CH:19]=[C:18]([C:20]4[CH:25]=[CH:24][C:23]([CH2:26][Cl:30])=[CH:22][CH:21]=4)[NH:17][C:13]=3[N:14]=[CH:15][N:16]=2)=[CH:5][CH:4]=1

Participants

6

Procedure

A suspension of 3.28 g (9.1 mMol) of {4-[4-(6-methoxy-pyridin-3-ylmethylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl]-phenyl}-methanol in 40 ml of acetonitrile, 40 ml of dioxane and 4 ml of SOCl2 is stirred for 1 h at RT. The mixture is dissolved in EtOAc and NaHCO3-solution, the aqueous layer separated off and extracted with EtOAc. The organic layers are washed with NaHCO3-solution, water and brine, dried (Na2SO4) and partially concentrated. The crystallized title compound can be filtered off, elemental analysis for C, H, and N, within 0.4%; of calculated value.

Workup

  1. customNaHCO3-solution, the aqueous layer separated off
  2. extractionextracted with EtOAc
  3. washThe organic layers are washed with NaHCO3-solution, water and brine
  4. dry with materialdried (Na2SO4)
  5. concentrationpartially concentrated
  6. customThe crystallized title compound
  7. filtrationcan be filtered off

Sources & evidence

ORD record
ord-8fe0af9c6132493d8fad7440912e5603
Source dataset
uspto-grants-2008_06
Patent number
US07390805B2

Reaction notes

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