Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441915Generated: November 2, 2026

Triethylamine → HCID 45095725, compound

https://huagongshe.com/reaction/1441915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantHCID 15545851HCID 15545851—
Solventtert-ButanolHCID 6386—
ProductHCID 45095725HCID 4509572559%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 1-cyclopentyl-3-ethyl-1H-indazole-6-carboxylic acid (258 mg) and triethylamine (0.56 mL) in t-butanol (1 ml) was added diphenylphosphoryl azide (0.33 mL). The mixture was stirred at 100° C. for 4 h, then partitioned between water (25 mL) and ether (25 mL). The ether layer was collected, dried (MgSO4), and passed through a plug of silica. The silica was washed with an additional 25 mL of ether and the mixture was concentrated in vacuo. The residue was dissolved in THF (5 mL) and 6N aq. HCL (1 mL) was added and the mixture was stirred for 18 h. Ether (25 mL) and water (25 mnL) were added and the ether layer was collected, dried (MgSO4), and concentrated in vacuo. The residue was purified by column chromatography on silica gel to yield 0.14 g of 6-amino-1-cyclopentyl-3-ethyl-1H-indazole (59% yield). 1H NMR (300 MHz) δ 7.45 (d, J=8.4 Hz, 1H), 6.52 (m,2H), 4.74 (p,J=7.8 Hz, 1H), 3.86 (br,2H), 2.95 (q,J=7.7 Hz, 2H), 2.3-1.8 (m,6H), 1.8-1.6 (m,2H), 1.37 (t,J=7.7 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655802B2
Source datasetuspto-grants-2010_02
ORD IDord-649f1567de414450aba58bb4d5e096a1
Source noteuspto-grants-2010_02