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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643716Generated: October 30, 2026

Methylamine → HCID 57708177, compound

https://huagongshe.com/reaction/643716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantHCID 68615718HCID 68615718—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 57708177HCID 5770817717%

Reaction Steps

To a solution of 2-{[1-(cyclopropylmethyl)-2-(2,2-dimethylpropyl)-1H-benzimidazol-5-yl]sulfonyl}-2-methylpropan-1-amine (Step K of Example 13, 177 mg, 0.469 mmol) and triethylamine (131 μL, 0.938 mmol) in dichloromethane (4 mL) was added p-nitrophenyl chloroformate (104 mg, 0.516 mmol) at room temperature. After stirring for 30 min, methylamine (40% aqueous solution, 3 mL) was added to the mixture and the whole was stirred for 2 h. To the resulting mixture was added ethyl acetate and 2 mol/L sodium hydroxide aqueous solution. The organic layer was dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by HPLC (ODS, gradient elution with Acetonitrile 10.01% aq. NH3=4:96 to 96:4, by volume; flow rate 40 mL/min) to afford the title compound (34 mg, 17%) as an amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700618B2
Source datasetuspto-grants-2010_04
ORD IDord-7a60c0196f5a45d38896224a7c44494e
Source noteuspto-grants-2010_04