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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387558Generated: November 4, 2026

Acetyl chloride → [4-(3-Acetylamino-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl ester

https://huagongshe.com/reaction/2387558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant[4-(3-Amino-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl esterHCID 59152902—
SolventTetrahydrofuranHCID 8028—
Product[4-(3-Acetylamino-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl esterHCID 5915291872.2%

Reaction Steps

To a solution of [4-(3-amino-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl ester (30 mg, 0.079 mmol) and acetyl chloride (9.2 mg, 0.119 mmol) in tetrahydrofuran (3 mL) was added triethylamine (16 mg, 0.158 mmol) at 0° C. After being stirred at room temperature overnight, the mixture was concentrated in vacuo. The residue was purified by flash column (gradient elution, 0-5% methanol in dichloromethane) to afford [4-(3-acetylamino-benzenesulfonylamino)-4,5,6,7-tetrahydro-indazol-1-yl]-acetic acid ethyl ester (24 mg, 72%) as a white solid. MS cald. for C19H24N4O5S 420, obsd. (ESI+) [(M+H)+] 421.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268870B2
Source datasetuspto-grants-2012_09
ORD IDord-35c90538c8014e7ea2d8e6cd01b6f5df
Source noteuspto-grants-2012_09