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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477495Generated: October 29, 2026

Methanesulfonyl chloride → HCID 14838661, compound

https://huagongshe.com/reaction/477495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 19804337HCID 19804337—
SolventDichloromethaneHCID 6344—
ProductHCID 14838661HCID 14838661109.7%

Reaction Steps

A solution of 5-amino-N-(1-ethyl-2-pyrrolidinylmethyl)-2,3-dihydrobenzo[b]furan-7-carboxamide (161) (1.80 g, 6.2 mmol) and methanesulfonyl chloride (12.78 g, 0.11 mol) in 30 ml of methylene chloride was heated to reflux overnight. The solution was diluted with CH2Cl2 (30 ml), and then extracted with water (2×30 ml). The combined aqueous layers were made basic with NaHCO3 powder, and extracted with CH2Cl2 (4×50 ml). The organic extracts were combined, dried over anhydrous Na2SO4, and evaporated to give crude 16n (2.5 g, 98.8%). This was recrystallized from EtOH/charcoal to afford 1.70 g of amide as a white solid, mp 180°-182° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04888353
Source datasetuspto-grants-1989_12
ORD IDord-4ac6ff6cfd9846b89f8c06e3cdc3394f
Source noteuspto-grants-1989_12