Potassium Carbonate → HCID 12150197, compound

HRID 991527Notes

Reaction equation

HRID 991527 reaction equation
Cl[CH2:2][C:3]1[N:12]=[C:11]([C:13]2[CH:18]=[CH:17][C:16]3[O:19][CH2:20][O:21][C:15]=3[CH:14]=2)[C:10]2[C:5](=[CH:6][C:7]3[O:24][CH2:23][O:22][C:8]=3[CH:9]=2)[N:4]=1.[SH:25][C:26]1[N:27]([CH3:31])[CH:28]=[CH:29][N:30]=1.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[CH3:31][N:27]1[CH:28]=[CH:29][N:30]=[C:26]1[S:25][CH2:2][C:3]1[N:12]=[C:11]([C:13]2[CH:18]=[CH:17][C:16]3[O:19][CH2:20][O:21][C:15]=3[CH:14]=2)[C:10]2[C:5](=[CH:6][C:7]3[O:24][CH2:23][O:22][C:8]=3[CH:9]=2)[N:4]=1

Participants

5

Procedure

A suspension of 2-chloromethyl-6,7-methylenedioxy-4-(3,4-methylenedioxy-phenyl)quinazoline (193 mg, 0.61 mmol) and 2-mercapto-1-methylimidazole (80 mg, 0.7 mmol) in dry DMF (2 mL) was treated with K2CO3 (97 mg, 0.7 mmol). The mixture was stirred at rt for 2 h, and then it was poured into ice-water. The mixture were extracted with EtOAc and the extract was washed with water and brine, dried over anhydrous MgSO4, and evaporated to yield the crude product, which was crystallized from EtOAc-hexane to give the title compound as colorless rods (142 mg); mp 155-160° C.; 1H NMR (CDCl3) 7.36 (s, 1H), 7.27 (s, 1H), 7.17 (d, J=7.7, 1H), 7.16 (s, 1H), 7.09 (s, 1H), 6.95 (d, J=7.7, 1H), 6.91 (s, 13H), 6.14 (s, 2H), 6.07 (s, 2H), 4.53 (s, 2H), 3,51 (s, 3H). Anal. calcd. for C21H16N4O4S: C, 59.99; H 3.84; N 13.33. Found: C, 59.78; H 3.82; N 13.20.

Workup

  1. extractionThe mixture were extracted with EtOAc
  2. washthe extract was washed with water and brine
  3. dry with materialdried over anhydrous MgSO4
  4. customevaporated
  5. customto yield the crude product, which
  6. customwas crystallized from EtOAc-hexane

Sources & evidence

ORD record
ord-1179f6a7c5024bcebc2ea455027bcd6e
Source dataset
uspto-grants-2002_10
Patent number
US06465472B1

Reaction notes

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