Methyl 6-(benzenesulfonylmethyl)-3-bromo-2-methoxybenzoate → 6-(Benzenesulphonylmethyl)-3-bromo-2-methoxybenzoic acid

HRID 2177794Notes

Reaction equation

HRID 2177794 reaction equation
C1(S(CC2C(C(O)=O)=C(NCCNC(OC(C)(C)C)=O)C(C3C=COC=3)=CC=2)(=O)=O)C=CC=CC=1.[C:36]1([S:42]([CH2:45][C:46]2[C:51]([C:52]([O:54]C)=[O:53])=[C:50]([O:56][CH3:57])[C:49]([Br:58])=[CH:48][CH:47]=2)(=[O:44])=[O:43])[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1>>[C:36]1([S:42]([CH2:45][C:46]2[C:51]([C:52]([OH:54])=[O:53])=[C:50]([O:56][CH3:57])[C:49]([Br:58])=[CH:48][CH:47]=2)(=[O:44])=[O:43])[CH:37]=[CH:38][CH:39]=[CH:40][CH:41]=1

Participants

3

Reactant 2

HCID 66685730Methyl 6-(benzenesulfonylmethyl)-3-bromo-2-methoxybenzoate2×HCID 671077416-(Benzenesulphonylmethyl)-2-[2-(t-butoxycarbonylamino)ethylamino]-3-(furan-3-yl)benzoic acid

Product 1

HCID 529139736-(Benzenesulphonylmethyl)-3-bromo-2-methoxybenzoic acid

Procedure

Prepared by proceeding in a similar manner to Intermediate 121, starting from methyl 6-(benzenesulphonylmethyl)-3-bromo-2-methoxybenzoate (Intermediate 65).

Workup

  1. customPrepared

Sources & evidence

ORD record
ord-f2fac1cd2a034fd182f6a7e386faa1a9
Source dataset
uspto-grants-2015_06
Patent number
US09067905B2

Reaction notes

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