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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161724Generated: October 30, 2026

5-Tert-butyl-3-isocyanato-1,2-oxazole → HCID 24889893, compound

https://huagongshe.com/reaction/1161724

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Tert-butyl-3-isocyanato-1,2-oxazoleHCID 12918838—
ReactantHCID 44598673HCID 44598673—
SolventTolueneHCID 1140—
ProductHCID 24889893HCID 2488989391.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of ethyl 3-[2-(4-aminophenyl)imidazo[2,1-b][1,3]benzothiazol-7-yl]propanoate (3.80 g, 10.4 mmol) from Step C and 5-tert-butyl-3-isocyanatoisoxazole (2.08 g, 12.5 mmol) in toluene (80 mL) was heated at 110° C. over night. A precipitate was formed, collected by filtration, washed with ether, and dried under high vacuum to give the title compound as a white solid (5.056 g, 91%). 1H NMR (DMSO-d6) δ 9.62 (s, 1H), 9.08 (s, 1H), 8.70 (s, 1H), 7.91 (s, 1H), 7.89 (d, 1H), 7.79 (d, 2H), 7.54 (d, 2H), 7.46 (d, 1H), 6.53 (s, 1H), 4.06 (q, 2H), 2.98 (t, 2H), 2.70 (t, 2H), 1.30 (s, 9H), 1.15 (t, 3H); LC-MS: ESI 532 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820657B2
Source datasetuspto-grants-2010_10
ORD IDord-6858f9e12c984d41b44d0f16f9fe43a5
Source noteuspto-grants-2010_10