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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471591Generated: October 30, 2026

Chlorosulfamic acid → 2-Sulfamoylamino-6-(2-methylprop-1-enyl)benzonitrile

https://huagongshe.com/reaction/471591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfamic acidHCID 24499—
Reactant2-Amino-6-(2-methylprop-1-enyl)benzonitrileHCID 67399767—
SolventDimethylacetamideHCID 31374—
Product2-Sulfamoylamino-6-(2-methylprop-1-enyl)benzonitrileHCID 6739996893%

Reaction Steps

A solution of 2-amino-6-(2-methylprop-1-enyl)benzonitrile (Example 129b) (1.24 g; 7.23 mmol) in N,N-dimethylacetamide (DMA) (20.0 mL), under a nitrogen atmosphere, was treated with sulfamoyl chloride (1.67 g; 14.45 mmol) at room temperature. The obtained mixture was stirred at room temperature for 2 h and the reaction was quenched with water (40 mL). The mixture was extracted with EtOAc (4×80 mL), the combined extract was washed with water (2×20 mL) and brine, and dried with MgSO4. The filtrate was evaporated and the residue was purified by chromatography on silica gel using gradient (Hexanes/EtOAc 1:0 to 1:1), to give 1.69 g (93%) of the title compound as a white solid. 1H-NMR (400 MHz, DMSO-d6) δ 9.42 (broad s, 1H), 7.61 (t, J=8.0 Hz, 1H), 7.44 (d, J=8.0 Hz, 1H), 7.24 (broad s, 2H), 7.19 (d, J=8.0 Hz, 1H), 6.35 (broad s, 1H), 1.92-1.95 (m, 3H), 1.76-1.79 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633186B2
Source datasetuspto-grants-2014_01
ORD IDord-dcb6921dc9f647d18c8854b8e076d5a8
Source noteuspto-grants-2014_01