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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069026Generated: November 1, 2026

Water → tert-Butyl (4-(2-hydroxyethyl)pyridin-2-yl)carbamate

https://huagongshe.com/reaction/2069026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactant(2-Boc-amino-pyridin-4-yl)-acetic acid ethyl esterHCID 53419364—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl (4-(2-hydroxyethyl)pyridin-2-yl)carbamateHCID 5841676770.5%

Reaction Conditions

Temperature-69 °C

Reaction Steps

To a solution of ethyl 2-(2-(tert-butoxycarbonylamino)pyridin-4-yl)acetate (19) (WO 2007089512) (10.0 g, 35.7 mmol) under nitrogen in THF (100 mL), at −78° C., was added DIBAL (1M solution in THF, 71.3 mL, 71.3 mmol) over 1 hr. The reaction mixture was stirred at −78 to −60° C. for 40 min and then warmed to −15° C. over 1 hr. The solution was re-cooled to −78° C. and treated with further DIBAL (1M solution in THF, 35 mL, 35.7 mmol). The mixture was allowed to warm to −40° C. and stirred for 1 hr. Water (10 mL) was added cautiously to quench the reaction followed by MgSO4 (20 g) and the solids removed by filtration. The filtrate was evaporated to dryness in vacuo and the residue subjected to column chromatography (SiO2, 330 g, 65% EtOAc in hexanes) to give the title compound (20) (6.00 g, 64%) as a yellow solid: m/z 239 (M+H)+ (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299073B2
Source datasetuspto-grants-2012_10
ORD IDord-f621b5cb181f4af7a74524ebac6fce7f
Source noteuspto-grants-2012_10