Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368444Generated: November 2, 2026

Cyclopropanecarbohydrazide → HCID 57513752, compound

https://huagongshe.com/reaction/2368444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarbohydrazideHCID 81396—
ReactantMethyl N-(triethylammoniosulfonyl)carbamateHCID 2724994—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 57476901HCID 57476901—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57513752HCID 57513752—

Reaction Conditions

Temperature150 °C

Reaction Steps

To a stirred solution of 2-(2-(4-Fluorobenzamido)-2-methylpropanamido)-4-(4-fluorophenyl)thiazole-5-carboxylic acid (100 mg, 0.224 mmol) and cyclopropanecarbohydrazide (27 mg, 0.27 mmol) were added HATU (128 mg, 0.34 mmol) and TEA (78 uL, 0.56 mmol). Volatiles were removed in vacuo. The residue was taken up in EtOAc and washed with 1N HCl (2×10 mL) followed by sat. NaHCO3 (2×10 mL). Organic layer was dried over magnesium sulfate and filtered. The filtrate was concentrated to dryness to afford a solid. The solid was dissolved in THF (5 mL) and treated with Burgess reagent (68 mg, 0.28 mmol) and heated in microwave at 150° C. for 30 minutes. Purification by silica gel chromatography (30-45% EtOAc/Heptanes) gave the title compound. 1H NMR (400 MHz, DMSO-d6) 0.82 (dd, J=4.74, 2.59 Hz, 3H) 1.08 (dd, J=8.34, 2.78 Hz, 3H) 2.19 (s, 1H) 7.33 (t, J=8.91 Hz, 3H) 7.25 (t, J=8.91 Hz, 3H) 7.71 (dd, J=8.84, 5.56 Hz, 3H) 8.03 (dd, J=8.78, 5.62 Hz, 3H) 8.65 (s, 1H) 12.61 (s, 1H). MS m/z 510.4 (M+H), 508.4 (M−1). HRMS cald for C25H18N2O4S=509.1333, found=509.1334. (M+H)+ 510.4, Rt=1.37 min, method A.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703761B2
Source datasetuspto-grants-2014_04
ORD IDord-bc575e3f79de49e5a6fae76de037ea42
Source noteuspto-grants-2014_04