Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235933Generated: October 31, 2026

Methanol → HCID 59300465, compound

https://huagongshe.com/reaction/2235933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantLithium HydroxideHCID 3939—
ReactantHCID 59300550HCID 59300550—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59300465HCID 5930046588%

Reaction Steps

To a solution of ethyl [(1S)-5-(3-{[6-(4-methoxyphenyl)-5-(trifluoromethyl)-2-pyridinyl]amino}propoxy)2,3-dihydro-1H-inden-1-yl]acetate (Example 304, 0.05 g, 0.09 mmol) in a mixture of THF (1 mL), methanol (1 mL), and water (0.5 mL) was added LiOH (0.02 g, 0.85 mmol). The mixture was stirred at rt for 18 h, and then concentrated under reduced pressure. The residue was taken up in water and acidified with 5% H3PO4. The aqueous solution was extracted with ethyl acetate. The combined organic phases dried (Na2SO4), filtered, and concentrated under reduced pressure to give the product (0.038 g, 88%). 1H NMR (400 MHz, CD2Cl2) δ 7.65 (d, 1H), 7.35 (d, 2H), 7.05 (d, 1H), 6.92 (d, 2H), 6.73 (s, 1H), 6.66 (dd, 1H), 6.49 (d, 1H), 4.02 (t, 2H), 3.84 (s, 3H), 3.55 (t, 3H), 3.45 (qt, 1H), 2.92-2.65 (m, 3H), 2.40-2.30 (m, 2H), 2.10-2.02 (m, 2H), 1.80-1.68 (m, 1H); LC-MS: RT=3.02 min, (M+H)+ 531.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714004B2
Source datasetuspto-grants-2010_05
ORD IDord-b8bc3269321541f8bea56a39d531bcca
Source noteuspto-grants-2010_05