Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427397Generated: October 27, 2026

(1R,2R)-2-{[4-(3-fluoro-4-{[6-(trifluoromethoxy)-1,3-benzothiazol-2-yl]amino}phenyl)phenyl]carbonyl}cyclopentane-1-carboxylic acid → (1R,2R)-2-({4'-[(5-methyl-1,3-benzoxazol-2-yl)amino]-1,1'-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid

https://huagongshe.com/reaction/2427397

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1R,2R)-2-{[4-(3-fluoro-4-{[6-(trifluoromethoxy)-1,3-benzothiazol-2-yl]amino}phenyl)phenyl]carbonyl}cyclopentane-1-carboxylic acidHCID 11444140—
ReactantN-(4-Bromophenyl)-5-methyl-1,3-benzoxazol-2-amineHCID 21985825—
Reactant(1R,2R)-Methyl 2-(4-bromobenzoyl)cyclopentanecarboxylateHCID 58681296—
Product(1R,2R)-2-({4'-[(5-methyl-1,3-benzoxazol-2-yl)amino]-1,1'-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acidHCID 1138514417%

Reaction Steps

This compound was prepared from N-(4-bromophenyl)-N-(5-methyl-1,3-benzoxazol-2-yl)amine (0.50 g, 1.65 mmol), methyl (1R,2R)-2-(4-bromobenzoyl)cyclopentanecarboxylate (0.57 g, 1.83 mmol, 94.5% ee) in a similar manner to the method described for (1R,2R)-2-({3′-fluoro-4′-[(6-trifluoromethoxy-1,3-benzothiazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid. Yield: 17%. 1H NMR (400 MHz, DMSO-d6) δ 10.80 (s, 1 H), 8.05 (d, 2 H), 7.75-7.90 (m, 6 H), 7.35 (d, 1 H), 7.25 (s, 1 H), 6.95 (d, 1 H), 4.05 (q, 1 H), 3.20 (s, 1 H), 2.40 (s, 3 H), 2.15 (m, 1 H), 2.00 (m, 1 H), 1.55-1.80 (m, 4 H). LC-MS m/z 441.3 (MH+), ret. time 3.48 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968576B2
Source datasetuspto-grants-2011_06
ORD IDord-a31b522214dc4b728fdf0e72fdcc7f91
Source noteuspto-grants-2011_06