HCID 12535807, compound → HCID 12535808, compound

HRID 437441Notes

Reaction equation

HRID 437441 reaction equation
Cl.[CH:2]1([CH2:5][O:6][C:7]2[CH:15]=[CH:14][CH:13]=[CH:12][C:8]=2[C:9]([NH2:11])=[NH:10])[CH2:4][CH2:3]1.[O:16]=[C:17]1NC(C2C=CC=CC=2OCC=C)=N[CH:19]=[C:18]1[C:33]([O:35][CH2:36][CH3:37])=[O:34]>>[O:16]=[C:17]1[NH:11][C:9]([C:8]2[CH:12]=[CH:13][CH:14]=[CH:15][C:7]=2[O:6][CH2:5][CH:2]2[CH2:4][CH2:3]2)=[N:10][CH:19]=[C:18]1[C:33]([O:35][CH2:36][CH3:37])=[O:34]

Participants

3

Reactant 2

HCID 12535807HCID 12535807, compoundHCID 22462385HCID 22462385, compound

Product 1

HCID 12535808HCID 12535808, compound

Procedure

The title compound was prepared from 2-cyclopropylmethoxybenzamidine hydrochloride in a manner similar to that described for the preparation of ethyl 1,6-dihydro-6-oxo-2-(2-allyloxyphenyl)pyrimidine-5-carboxylate in Example 8. The product had m.p. 104°-105°.

Sources & evidence

ORD record
ord-17d86935973e41068a82e903e89b9399
Source dataset
uspto-grants-1977_06
Patent number
US04031093

Reaction notes

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