Dibutyltin oxide → HCID 178490276, compound

HRID 2110653Notes

Reaction equation

HRID 2110653 reaction equation
[CH3:1][O:2][C:3]1[N:8]=[C:7]([C:9]2[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=2)[C:12]#[N:13])[CH:6]=[C:5]([NH:17][CH2:18][CH2:19][C:20]2[CH:25]=[CH:24][C:23]([O:26][CH3:27])=[CH:22][CH:21]=2)[N:4]=1.C[Si]([N:32]=[N+:33]=[N-:34])(C)C.C([Sn](=O)CCCC)CCC>C1(C)C=CC=CC=1>[CH3:27][O:26][C:23]1[CH:22]=[CH:21][C:20]([CH2:19][CH2:18][NH:17][C:5]2[CH:6]=[C:7]([C:9]3[CH:16]=[CH:15][CH:14]=[C:11]([C:12]4[NH:34][N:33]=[N:32][N:13]=4)[CH:10]=3)[N:8]=[C:3]([O:2][CH3:1])[N:4]=2)=[CH:25][CH:24]=1

Participants

5

Procedure

A solution of 3-{2-methoxy-6-[2-(4-methoxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzonitrile [0.12 g, 0.33 mmol, Example 35(t)], trimethylsilylazide (0.22 mL, 1.65 mmol) and dibutyltinoxide (41 mg, 0.16 mmol) in toluene (5 mL) is heated to 95° C. for 6 hours. The reaction mixture is concentrated, and partitioned between water and ethyl acetate. The aqueous phase solution is acidified with dilute hydrochloric acid to pH, 3.0, and extracted with ethyl acetate. The extracts are dried over magnesium sulfate, filtered and concentrated. The residue is subjected to chromatography on silica gel eluting with 5% MeOH in DCM to afford [2-(4-methoxy-phenyl)-ethyl]-{2-methoxy-6-[3-(1H-tetrazol-5-yl)-phenyl]-pyrimidin-4-yl}-amine [60 mg, 45%, Example 24(a)]. LCMS: RT=2.65 minutes, MS: 404 (M+H).

Workup

  1. concentrationThe reaction mixture is concentrated
  2. custompartitioned between water and ethyl acetate
  3. extraction3.0, and extracted with ethyl acetate
  4. dry with materialThe extracts are dried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-413959a552e946e299dcf4eaba4fd349
Source dataset
uspto-grants-2009_04
Patent number
US07517889B2

Reaction notes

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