Hydrochloric Acid → HCID 15342560, compound
Reaction equation
Cl.[Cl:2][C:3]1[CH:4]=[C:5]([NH:13][CH2:14][C:15]([O:17][CH3:18])=[O:16])[C:6](=[CH:11][CH:12]=1)[C:7]([O:9]C)=O.[O-:19][C:20]#[N:21].[K+]>S1(CCCC1)(=O)=O>[Cl:2][C:3]1[CH:4]=[C:5]2[C:6]([C:7](=[O:9])[NH:21][C:20](=[O:19])[N:13]2[CH2:14][C:15]([O:17][CH3:18])=[O:16])=[CH:11][CH:12]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Hydrogen chloride is passed into 1 g of methyl 4-chloro-N-(methoxycarbonylmethyl)anthranilate and 1.6 g of potassium cyanate in 20 ml of sulfolane at 50° C. until analysis by HPLC indicates complete conversion. The product is precipitated by addition of water, filtered off, washed with water and dried. 0.59 g (57%) of methyl 1,2,3,4-tetrahydro-7-chloro-2,4-dioxoquinazolin-1-ylacetate is obtained.
Workup
- customThe product is precipitated by addition of water
- filtrationfiltered off
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-ea37c61992fb4c599b247a0301cafa8a
- Source dataset
- uspto-grants-1999_12
- Patent number
- US06001831
Reaction notes
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