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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478901Generated: November 2, 2026

tert-Butanol → HCID 67353089, compound

https://huagongshe.com/reaction/1478901

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 67355433HCID 67355433—
ProductHCID 67353089HCID 6735308926.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of diphenylphosphoryl azide (1.7 g, 6.2 mmol), Et3N (2.9 ml, 21 mmol) and 1-(cyclopropylmethyl)-1H-pyrrolo[3,2-c]pyridine-6-carboxylic acid (2B, 0.9 g, 4.0 mmol) in 2-methylpropan-2-ol (10 g, 140 mmol) was stirred at room temperature for 1 h and 80° C. for 3 h. The mixture was extracted with EtOAct/H2O. The organic layer was washed with brine, dried over MgSO4 and concentrated in vacuo. The crude mixture was purified by chromatography (SiO2, hexanes:EtOAc=50:50) to give tert-butyl 1-(cyclopropylmethyl)-1H-pyrrolo[3,2-c]pyridin-6-ylcarbamate (2C, 300 mg, 25% yield) as a white powder. 1 H NMR (400 MHz, CHLOROFORM-d) δ ppm 0.35-0.44 (m, 2 H) 0.57-0.70 (m, 2 H) 1.19-1.33 (m, 1 H) 1.57 (s, 9 H) 3.97 (d, J=6.82 Hz, 2 H) 6.52-6.54 (m, 1 H) 7.19 (d, J=3.28 Hz, 1 H) 7.59 (br. s., 1 H) 7.93 (s, 1 H) 8.56 (d, J=1.01 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403819B2
Source datasetuspto-grants-2016_08
ORD IDord-c02d60c9439a4a21aa68b6857f53a373
Source noteuspto-grants-2016_08