Sodium Hydroxide → HCID 21388808, compound

HRID 1833732Notes

Reaction equation

HRID 1833732 reaction equation
Cl.C(C1C=CC(C(N)=N)=CC=1)CC.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]([CH2:46][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]([CH2:46][CH2:47][CH3:48])=[CH:42][CH:41]=2)[N:36]=1

Participants

8

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-n-propylbenzamidine 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-n-propylphenyl)-pyrimidine (melting point 246.0°-247.6° C) is treated with phosphorus oxychloride to give 4-chloro-5-cyano-2-(4-n-propylphenyl)-pyrimidine having a melting point of 109.4°-109.7° C.

Workup

  1. customThe starting material can be obtained

Sources & evidence

ORD record
ord-59b3f3e1ffa74a72b253299d3cca3310
Source dataset
uspto-grants-1978_01
Patent number
US04066570

Reaction notes

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