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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415465Generated: October 30, 2026

Dimethylsulphamoyl chloride → HCID 69289960, compound

https://huagongshe.com/reaction/2415465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylsulphamoyl chlorideHCID 83372—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant2-Methyl-4-pyrrolidin-1-yl-quinolin-7-olHCID 135804118—
SolventDimethylformamideHCID 6228—
ProductHCID 69289960HCID 6928996029.8%

Reaction Steps

229.4 mg (1 mmol) of 2-methyl-4-pyrrolidin-1-yl-quinolin-7-ol, product of example 2, were suspended under an argon atmosphere in 20 ml of DMF, 0.6 g (1.2 mmol) of molecular sieves (4 nm) were added followed by 138 mg (1.2 mmol) of potassium tert-butoxide, and the mixture was stirred for 1 h at RT. It was then cooled to 0° C., treated with 0.13 ml (1.2 mmol) N,N-dimethylsulfamoyl chloride and stirred for 3 h at 0° C. The reaction mixture was partitioned between EtOAc and water, the aqueous layer was extracted twice with EtOAc, the combined organic layers were washed with water then with saturated NaCl solution, dried over magnesium sulphate and concentrated in vacuo. The residue was triturated with diethyl ether; the viscous oil obtained was filtered off by suction and dried in a high vacuum. Upon further triturating with heptane solid material was obtained which was dried in a high vacuum to give 100 mg (29.3%) of dimethyl-sulfamic acid 2-methyl-4-pyrrolidin-1-yl-quinolin-7-yl ester as an off-white solid. ISP mass spectrum, m/e: 336.2 (M+1 calculated for C16H21N3O3S: 336).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818767B2
Source datasetuspto-grants-2004_11
ORD IDord-bae9839df2a640cfb2a79dde5af29d89
Source noteuspto-grants-2004_11