Ethyl pyrazolo[1,5-a]pyrimidine-5-carboxylate → 2-Phenyl-pyrazolo-[1,5-a]-pyrimidine-5-carboxylic acid ethyl ester

HRID 1443844Notes

Reaction equation

HRID 1443844 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[CH:11]=[C:10](Cl)[N:9]2[N:13]=[C:14]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[CH:15]=[C:8]2[N:7]=1)=[O:5])[CH3:2].C(OC(C1C=CN2N=CC=C2N=1)=O)C>>[CH2:1]([O:3][C:4]([C:6]1[CH:11]=[CH:10][N:9]2[N:13]=[C:14]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[CH:15]=[C:8]2[N:7]=1)=[O:5])[CH3:2]

Participants

3

Reactant 2

HCID 49763022Ethyl pyrazolo[1,5-a]pyrimidine-5-carboxylateHCID 586284132-Phenyl-7-chloro-pyrazolo-[1,5-a]-pyrimidine-5-carboxylic acid ethyl ester

Product 1

HCID 586283142-Phenyl-pyrazolo-[1,5-a]-pyrimidine-5-carboxylic acid ethyl ester

Procedure

This compound was synthesized from 2-phenyl-7-chloro-pyrazolo-[1,5-a]-pyrimidine-5-carboxylic acid ethyl ester, according to the process for synthesizing the foregoing pyrazolo-[1,5-a]-pyrimidine-5-carboxylic acid ethyl ester. mp: 180-181° C.

Sources & evidence

ORD record
ord-d40c7742882f44369a97355c94a74cd3
Source dataset
uspto-grants-2010_02
Patent number
US07662826B2

Reaction notes

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