Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174078Generated: October 31, 2026

tert-Butyl 4-(5-cyanobenzo[d]oxazole-2-carbonyl)-5-methoxy-7-methyl-1H-indole-1-carboxylate → tert-butyl 4-(1-(5-cyanobenzo[d]oxazol-2-yl)-1-hydroxyethyl)-5-methoxy-7-methyl-1H-indole-1-carboxylate

https://huagongshe.com/reaction/2174078

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(5-cyanobenzo[d]oxazole-2-carbonyl)-5-methoxy-7-methyl-1H-indole-1-carboxylateHCID 86701711—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl 4-(1-(5-cyanobenzo[d]oxazol-2-yl)-1-hydroxyethyl)-5-methoxy-7-methyl-1H-indole-1-carboxylateHCID 86701712—

Reaction Steps

To a solution of tert-butyl 4-(5-cyanobenzo[d]oxazole-2-carbonyl)-5-methoxy-7-methyl-1H-indole-1-carboxylate (600 mg, 1.39 mmol) in THF (14 mL) at 0° C. methylmagnesium chloride, 3M in THF (1.39 mL, 4.17 mmol) was added. The reaction mixture was stirred for 15 min and then quenched with a saturated aq. solution of NH4Cl at 0° C. The layers were separated and the aqueous layer was extracted with EtOAc. The organic phase was dried over MgSO4 filtered and concentrated. The resulting residue was absorbed onto silica and purified by flash chromatography (0-50% EtOAc:heptanes) to give the title compound. MS (ESI+) m/z 448.22 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056874B2
Source datasetuspto-grants-2015_06
ORD IDord-ba9fa51435ab4589a8d0ca90b85cb36f
Source noteuspto-grants-2015_06