HCID 16641047, compound → HCID 10174350, compound

HRID 1063670Notes

Reaction equation

HRID 1063670 reaction equation
FC(F)(F)C1C=CC(COC2C=CC(CO)=CC=2)=CC=1.C[O:22][C:23](=[O:55])[CH2:24][O:25][C:26]1[CH:31]=[C:30]([O:32][CH3:33])[C:29]([S:34][CH2:35][C:36]2[CH:41]=[CH:40][C:39]([O:42][CH2:43][C:44]3[CH:49]=[CH:48][C:47]([C:50]([F:53])([F:52])[F:51])=[CH:46][CH:45]=3)=[CH:38][CH:37]=2)=[CH:28][C:27]=1[CH3:54]>>[CH3:33][O:32][C:30]1[C:29]([S:34][CH2:35][C:36]2[CH:37]=[CH:38][C:39]([O:42][CH2:43][C:44]3[CH:45]=[CH:46][C:47]([C:50]([F:53])([F:52])[F:51])=[CH:48][CH:49]=3)=[CH:40][CH:41]=2)=[CH:28][C:27]([CH3:54])=[C:26]([CH:31]=1)[O:25][CH2:24][C:23]([OH:55])=[O:22]

Participants

3

Reactant 2

HCID 16641047HCID 16641047, compoundHCID 20827053HCID 20827053, compound

Product 1

HCID 10174350HCID 10174350, compound

Procedure

The title compound was prepared in the manner analogous to Example 3B using 14A. MS m/z 265 (M-Cl+1). Step 3. Preparation of {5-Methoxy-2-methyl-4-[4-(4-trifluoromethyl-benzyloxy)-benzylsulfanyl]-phenoxy}-acetic acid methyl ester (Compound 14C)

Sources & evidence

ORD record
ord-a4392c15b9a24bb6bcc3e71f7d6b2061
Source dataset
uspto-grants-2005_11
Patent number
US06964983B2

Reaction notes

Loading…