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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541757Generated: November 2, 2026

tert-Butanol → HCID 57962653, compound

https://huagongshe.com/reaction/541757

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantDiphenylphosphoryl azideHCID 123414—
ReactantHCID 57961678HCID 57961678—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 57962653HCID 5796265355%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of 6-chloro-2,4,8,22-tetraazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaene-11-carboxylic acid (9.2 mg, 25.1 μmol) in tert-butyl alcohol (0.16 mL) was added triethylamine (3.5 μL, 25.1 μmol) and diphenylphosphonic azide (5.4 μL, 25.1 μmol). The resulting mixture was heated at 85° C. overnight. The reaction mixture was diluted with DMSO and purified with preparative LCMS to give the desired product (6 mg, 55%). 1H NMR (400 MHz, DMSO-d6): δ 9.33 (s, 1H), 9.22 (s, 1H), 8.09 (s, 1H), 7.92 (s, 1H), 7.31 (m, 2H), 7.08 (t, 1H), 7.03 (s, 1H), 6.88 (dd, 1H), 6.80 (dd, 1H), 2.80 (d, 4H), 1.46 (s, 9H). LCMS calculated for C23H25ClN5O2(M+H)+: m/z=438.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-069317e56b5741c08300fe54a2d3dbb5
Source noteuspto-grants-2014_10