2-Hydroxybenzonitrile → HCID 178516965, compound

HRID 869433Notes

Reaction equation

HRID 869433 reaction equation
COC(=O)[CH:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[C:12](OC)=[O:13])Br.COC(=O)C(C1C=CC(Cl)=CC=1C(OC)=O)Br.[Cl:34][C:35]1[CH:36]=[CH:37][C:38]([OH:43])=[C:39]([CH:42]=1)[C:40]#[N:41].OC1C=CC=CC=1C#N>>[OH:13][C:12]1[C:7]2[C:6](=[CH:11][CH:10]=[CH:9][CH:8]=2)[C:4]2[O:43][C:38]3[CH:37]=[CH:36][C:35]([Cl:34])=[CH:42][C:39]=3[C:40]=2[N:41]=1

Participants

5

Reactant 4

HCID 119072-HydroxybenzonitrileHCID 27774205-Chloro-2-hydroxybenzonitrileHCID 115075112-(2-Methoxycarbonyl-phenyl)-2-bromo-acetic acid methyl esterHCID 867222712-(4-Chloro-2-methoxycarbonyl-phenyl)-2-bromo-acetic acid methyl ester

Product 1

HCID 178516965HCID 178516965, compound

Procedure

The procedure was similar to step S19B, while the starting material was 24A in stead of 19A, and used 5-chloro-2-hydroxy-benzonitrile in stead of 2-hydroxy-benzonitrile.

Sources & evidence

ORD record
ord-7560b16d99a9434289dc7e72084804c6
Source dataset
uspto-grants-2015_03
Patent number
US08969373B2

Reaction notes

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