Water → HCID 57986847, compound

HRID 2063439Notes

Reaction equation

HRID 2063439 reaction equation
Cl.[N:2]1([C:7]2[CH:25]=[CH:24][C:10]([O:11][CH2:12][C:13]3[N:14]=[C:15]([CH:18]4[CH2:23][CH2:22][CH2:21][NH:20][CH2:19]4)[S:16][CH:17]=3)=[CH:9][CH:8]=2)[CH:6]=[N:5][N:4]=[N:3]1.ClC1N=[CH:31][CH:30]=[CH:29][N:28]=1.[C:33]([O-])(O)=O.[Na+].O.C[N:40]([CH:42]=O)[CH3:41]>>[CH2:31]([C:30]1[CH:41]=[N:40][C:42]([N:20]2[CH2:21][CH2:22][CH2:23][CH:18]([C:15]3[S:16][CH:17]=[C:13]([CH2:12][O:11][C:10]4[CH:9]=[CH:8][C:7]([N:2]5[CH:6]=[N:5][N:4]=[N:3]5)=[CH:25][CH:24]=4)[N:14]=3)[CH2:19]2)=[N:28][CH:29]=1)[CH3:33]

Participants

6

Reactant 5

HCID 962WaterHCID 6228DimethylformamideHCID 744042-ChloropyrimidineHCID 516892Sodium BicarbonateHCID 68663147HCID 68663147, compound

Product 1

HCID 57986847HCID 57986847, compound

Conditions

Temperature
90 °C

Procedure

A mixture of 3-[4-(4-Tetrazol-1-yl-phenoxymethyl)-thiazol-2-yl]-piperidine hydrochloride (150 mg, 0.407 mmol), 2-chloropyrimidine (0.074 mL, 2.0 eq.) and NaHCO3 (171 mg, 2.03 mmol) in DMF (5 mL) was heated at 90° C. for 4 hours. Water was added and the solution was extracted with ethyl acetate, separated, dried over sodium sulfate, filtered and concentrated. The residue was purified on silica gel (50:50 EtOAc/hexanes) to afford the desired product. 1H NMR (CDCl3): δ 8.91 (1H, s), 8.19 (2H, s), 7.63 (2H, m), 7.26(1H, s), 7.17 (2H, m), 5.25 (2H, s), 4.97 (1H, m), 4.62 (1H, m), 3.25 (2H, m), 3.07 (1H, m), 2.46 (2H, q), 2.28(1H, m), 1.88 (2H, m), 1.68 (1H, m), 1.20 (3H, t).

Workup

  1. extractionthe solution was extracted with ethyl acetate
  2. customseparated
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe residue was purified on silica gel (50:50 EtOAc/hexanes)

Sources & evidence

ORD record
ord-7c671f95bd62418cb7c556dba4fbc7e1
Source dataset
uspto-grants-2012_10
Patent number
US08288384B2

Reaction notes

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