2-Methyl-2-({1-[6-(2,2,2-trifluoro-ethoxy)-pyridin-3-ylmethoxy]-naphthalene-2-carbonyl}-amino)-propionic acid → 2-Methyl-2-({1-[6-(2,2,2-trifluoro-ethoxy)-pyridin-3-ylmethoxy]-naphtha-lene-2-carbonyl}-amino)-butyric acid
Reaction equation
CC(NC(C1C=CC2C(=CC=CC=2)C=1OCC1C=NC(OCC(F)(F)F)=CC=1)=O)(C)C(O)=O.C[O:35][C:36](=[O:68])[C:37]([CH3:67])([NH:40][C:41]([C:43]1[CH:52]=[CH:51][C:50]2[C:45](=[CH:46][CH:47]=[CH:48][CH:49]=2)[C:44]=1[O:53][CH2:54][C:55]1[CH:56]=[N:57][C:58]([O:61][CH2:62][C:63]([F:66])([F:65])[F:64])=[CH:59][CH:60]=1)=[O:42])[CH2:38][CH3:39]>>[CH3:67][C:37]([NH:40][C:41]([C:43]1[CH:52]=[CH:51][C:50]2[C:45](=[CH:46][CH:47]=[CH:48][CH:49]=2)[C:44]=1[O:53][CH2:54][C:55]1[CH:56]=[N:57][C:58]([O:61][CH2:62][C:63]([F:66])([F:65])[F:64])=[CH:59][CH:60]=1)=[O:42])([CH2:38][CH3:39])[C:36]([OH:68])=[O:35]Participants
3
Reactant 2
Product 1
Procedure
2-Methyl-2-({1-[6-(2,2,2-trifluoro-ethoxy)-pyridin-3-ylmethoxy]-naphtha-lene-2-carbonyl}-amino)-butyric acid was prepared in similar manner as 2-methyl-2-({1-[6-(2,2,2-trifluoro-ethoxy)-pyridin-3-ylmethoxy]-naphthalene-2-carbonyl}-amino)-propionic acid (example 150) via 2-methyl-2-({1-[6-(2,2,2-trifluoro-ethoxy)-pyridin-3-ylmethoxy]-naphthalene-2-carbonyl}-amino)-butyric acid methyl ester (C25H25F3N2O5 (490.48), LCMS (ESI): 491.15 (MH+)).
Sources & evidence
- ORD record
- ord-6c7b68bb79304244a28a39768a7fd110
- Source dataset
- uspto-grants-2011_04
- Patent number
- US07919628B2
Reaction notes
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