Ammonia → 4-(alpha-Carbamoyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline

HRID 2392866Notes

Reaction equation

HRID 2392866 reaction equation
[NH3:1].C([O:4][C:5]([CH:7]([NH:17][C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[C:25]([Cl:28])[CH:26]=2)[N:21]=[CH:20][N:19]=1)[C:8]1[CH:13]=[CH:12][C:11]2[O:14][CH2:15][O:16][C:10]=2[CH:9]=1)=O)C>C(O)C>[C:5]([CH:7]([NH:17][C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[C:25]([Cl:28])[CH:26]=2)[N:21]=[CH:20][N:19]=1)[C:8]1[CH:13]=[CH:12][C:11]2[O:14][CH2:15][O:16][C:10]=2[CH:9]=1)(=[O:4])[NH2:1]

Participants

4

Reactant 2

HCID 222AmmoniaHCID 18796707HCID 18796707, compound

Product 1

HCID 187967044-(alpha-Carbamoyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

20 ml of a 10% solution of ammonia in ethanol was added to 200 mg of 4-(α-ethoxycarbonyl-3,4-methylenedioxybenzyl)amino-6-chloroquinazoline. The obtained mixture was stirred at room temperature for 3 days. The crystal thus precipitated was recovered by filtration. Thus, 60 mg of the title compound was obtained.

Workup

  1. customThe crystal thus precipitated
  2. filtrationwas recovered by filtration

Sources & evidence

ORD record
ord-2e6aac06acb845ab9c63e207a32f4fde
Source dataset
uspto-grants-1998_09
Patent number
US05801180

Reaction notes

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