Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175738Generated: November 2, 2026

(Chloromethyl)sulfonyl chloride → HCID 59559694, compound

https://huagongshe.com/reaction/1175738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Chloromethyl)sulfonyl chlorideHCID 77054—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(2,3-dihydro-1H-indol-5-yl)-5-vinyl-3H-imidazo[4,5-b]pyridineHCID 59559714—
SolventDichloromethaneHCID 6344—
ProductHCID 59559694HCID 5955969498.3%

Reaction Steps

A solution of 3-(2,3-dihydro-1H-indol-5-yl)-5-vinyl-3H-imidazo[4,5-b]pyridine (2.57 g, 9.80 mmol) (Intermediate 10.1), chloromethanesulfonyl chloride (2.00 ml, 19.59 mmol), and N,N-diisopropylethylamine (11.98 ml, 68.58 mmol) in dichloromethane (100 ml) is stirred for 20 min at ambient temperature. The mixture is successively extracted with saturated aqueous ammonium chloride and saturated aqueous sodium bicarbonate. The organic layer is dried over sodium sulfate and concentrated in vacuo to give 3.61 g (98%) of the respective sulfonamide. HPLC (over 10 min 10-85% MeCN/100 mM aq. NaOAc): 92% purity, tR 8.05 min (tR(SM) 6.64 min). 1H-NMR (400 MHz, DMSO-d6) δ 9.03 (s, 1H), 8.22 (d, 1H), 7.85 (s, 1H), 7.79 (d, 1H), 7.56 (m, 2H), 6.93 (dd, 1H), 6.25 (d, 1H), 5.50 (d, 1H), 5.41 (s, 2H), 4.21 (t, 2H), 3.28 (t, 2H) ppm. MS (ESI) m/z (C17H15ClN4O2S) 375.0 (M+1, 100) Finnegan LCQ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842698B2
Source datasetuspto-grants-2010_11
ORD IDord-7c932afa70d24053a63b530448e8f47c
Source noteuspto-grants-2010_11