Sodium Hydroxide → HCID 21388851, compound
Reaction equation
Cl.C(OC1C=CC(C(N)=N)=CC=1)C.C(OC(=O)C(=COCC)C#N)C.CC[O-].[Na+].[OH-].[Na+].[C:32]([C:34]1[C:35](O)=[N:36][C:37]([C:40]2[CH:45]=[CH:44][C:43]([O:46][CH2:47][CH3:48])=[CH:42][CH:41]=2)=[N:38][CH:39]=1)#[N:33].P(Cl)(Cl)([Cl:52])=O>C(O)C>[Cl:52][C:35]1[C:34]([C:32]#[N:33])=[CH:39][N:38]=[C:37]([C:40]2[CH:45]=[CH:44][C:43]([O:46][CH2:47][CH3:48])=[CH:42][CH:41]=2)[N:36]=1Participants
8
Reactant 6
Product 1
Reagents, catalysts & solvents 1
Procedure
The starting material can be obtained according to the procedure of A. R. Todd and F. Bergel, J. Chem. Soc. 1937, 365 by reaction of p-ethoxybenzamidine hydrochloride with α-ethoxymethylene- α-cyanoacetic acid ethyl ester and sodium ethylate in ethanol and then with sodium hydroxide solution. The resulting 5-cyano-4-hydroxy-2-(4-ethoxyphenyl)-pyrimidine (melting point 288.6°-290.5° C) is treated with phosphorus oxychloride to give 4-chloro-5-cyano-2-(4-ethoxyphenyl)-pyrimidine having a melting point of 190.6°-192.4° C.
Workup
- customThe starting material can be obtained
Sources & evidence
- ORD record
- ord-b8f9ed140ab547bb84b40c4b63efb7f0
- Source dataset
- uspto-grants-1978_01
- Patent number
- US04066570
Reaction notes
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