Methyl 2-chloropyrimidine-5-carboxylate → HCID 66697039, compound

HRID 2096889Notes

Reaction equation

HRID 2096889 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[CH:4][C:3]=1[CH:9]([CH3:27])[C:10]([C:16]1[CH:17]=[CH:18][C:19]2[O:23][C:22](=[O:24])[N:21]([CH3:25])[C:20]=2[CH:26]=1)([OH:15])[C:11]([F:14])([F:13])[F:12].[CH3:28][O:29][C:30]([C:32]1[CH:33]=[N:34][C:35](Cl)=[N:36][CH:37]=1)=[O:31]>>[CH3:28][O:29][C:30]([C:32]1[CH:33]=[N:34][C:35]([O:8][C:6]2[CH:5]=[CH:4][C:3]([CH:9]([CH3:27])[C:10]([OH:15])([C:16]3[CH:17]=[CH:18][C:19]4[O:23][C:22](=[O:24])[N:21]([CH3:25])[C:20]=4[CH:26]=3)[C:11]([F:12])([F:13])[F:14])=[C:2]([Cl:1])[CH:7]=2)=[N:36][CH:37]=1)=[O:31]

Participants

3

Reactant 2

HCID 12627752Methyl 2-chloropyrimidine-5-carboxylateHCID 666969865-[2-(2-Chloro-4-hydroxy-phenyl)-1-hydroxy-1-trifluoromethyl-propyl]-3-methyl-3H-benzooxazol-2-one

Product 1

HCID 66697039HCID 66697039, compound

Procedure

The title compound was prepared in analogy to Example 196 from 5-[2-(2-chloro-4-hydroxy-phenyl)-1-hydroxy-1-trifluoromethyl-propyl]-3-methyl-3H-benzooxazol-2-one (obtained in Example 172) by alkylation with methyl-2-chloropyrimidine-5-carboxylate [CAS Reg. No. 287714-35-6]. MS (m/e)=538.2 [M+H+].

Sources & evidence

ORD record
ord-e1f4567498f348e8b7ab6119e0b88274
Source dataset
uspto-grants-2013_05
Patent number
US08450313B2

Reaction notes

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