Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512795Generated: November 3, 2026

Acetic Acid → HCID 59146163, compound

https://huagongshe.com/reaction/1512795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantGlycine ethyl esterHCID 12176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 59146184HCID 59146184—
SolventDichloromethaneHCID 6344—
ProductHCID 59146163HCID 5914616382.5%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a stirred solution of [7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-methyl-1H-indol-3-yl]acetaldehyde (D88) (20 mg), ethyl glycinate (10 mg) and acetic acid (0.1 mL) in DCM (10 mL) was added sodium triacetoxyborohydride (21 mg). The reaction was stirred at 20° C. for 1 h. The reaction mixture was partitioned between DCM (25 mL) and water (25 mL). The organic phase was evaporated to give ethyl N-{2-[7-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-1-methyl-1H-indol-3-yl]ethyl}glycinate (D89) as a brown oil (20 mg), which was used directly in the next hydrolysis step. MS (ES): C26H29ClN4O4 requires 496; found 497.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217028B2
Source datasetuspto-grants-2012_07
ORD IDord-ac8dd205d4c7465cb72a7553844b4089
Source noteuspto-grants-2012_07