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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405091Generated: October 31, 2026

tert-Butanol → HCID 67357244, compound

https://huagongshe.com/reaction/2405091

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 71087282HCID 71087282—
SolventDimethylformamideHCID 6228—
ProductHCID 67357244HCID 673572449.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of diphenylphosphoryl azide (4.3 g, 16 mmol), Et3N (7.3 ml, 52 mmol) and 3-bromo-1-ethyl-1H-pyrrolo[3,2-c]pyridine-6-carboxylic acid (3B, 2.8 g, 10 mmol) in DMF (30 ml) was stirred at 0° C. for 1 h. The mixture was extracted with EtOAc/H2O. The organic layer was washed with brine, dried over MgSO4 and concentrated in vacuo. The crude mixture was dissolved in toluene (30 ml) and added 2-methylpropan-2-ol (3.9 g, 52 mmol). The mixture was stirred at 70° C. for 2 h. The mixture was concentrated in vacuo and purified by chromatography (SiO2, hexanes:EtOAc=1:1) to give tert-butyl 3-bromo-1-ethyl-1H-pyrrolo[3,2-c]pyridin-6-ylcarbamate (3C, 340 mg, 0.99 mmol, 9.5% yield) as a white powder. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.35 (t, J=7.20 Hz, 3H) 1.49 (s, 9H) 4.14 (q, J=7.33 Hz, 2H) 7.60 (s, 1H) 7.83 (d, J=0.76 Hz, 1H) 8.36 (d, J=0.76 Hz, 1H) 9.59 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802695B2
Source datasetuspto-grants-2014_08
ORD IDord-a719868312ca4b47b686ffc22d1a0a7c
Source noteuspto-grants-2014_08