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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237627Generated: October 25, 2026

1-Hydroxybenzotriazole → HCID 178505181, compound

https://huagongshe.com/reaction/2237627

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 178486264HCID 178486264—
ReactantHCID 178508633HCID 178508633—
SolventEthyl AcetateHCID 8857—
ProductHCID 178505181HCID 178505181—

Reaction Steps

To a stirred solution of {trans-4-[4-(4-amino-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)phenyl]cyclohexyl}acetic acid (50 mg, 0.13 mmol), from Example 2, N-methylsulfonamide (30 mg, 0.32 mmol) were added HOBT (29 mg, 0.19 mmol), EDCl (30 mg, 0.32 mmol) and TEA (19.1 mg, 0.19 mmol). After 18 hours, the reaction mixture was diluted into EtOAc, washed with water, dried over sodium sulfate and concentrated in vacuo. Reverse-phase chromatography afforded the desired product as a white solid, 5.3 mg. 1H NMR (400 MHz, DMSO-d6): δ 8.17 (s, 1H), 7.64 (br s, 2H) 7.20 (s, 4H), 4.58 (m, 2H), 3.92 (m, 2H), 3.20 (s, 3H), 2.42 (m, 1H), 2.17 (m, 2H), 1.73 (m, 5H), 1.40 (m, 2H), 1.05 m, 2H). m/z=474.4 (M+1). IC50 44.5 nM (range 34.2-75.0 nM).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718645B2
Source datasetuspto-grants-2010_05
ORD IDord-19d5230fcd6f46449a40fcd54ed26180
Source noteuspto-grants-2010_05