Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385607Generated: October 26, 2026

Dimethylformamide → Pentyl methanesulfonate

https://huagongshe.com/reaction/1385607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant1,5-DiiodopentaneHCID 12354—
ReactantSodium hydrideHCID 24758—
ReactantRacemic 5-(4'-hydroxyphenyl)-7-(dimethylamino)tetrahydrobenzothiepine-1,1-dioxideHCID 22678846—
ProductPentyl methanesulfonateHCID 111883—

Reaction Steps

To a stirred solution of 231 mg (5.79 mmol, 60% disp.) of NaH in 22 mL of DMF was added 2.05 g (4.45 mmol) of 5-(4′-hydroxyphenyl)-7-(dimethylamino)tetra-hydrobenzothiepine-1,1-dioxide (obtained from Example 1402, Step 10), and the resulting solution was stirred at ambient temperature for 1 hour. To the mixture was added 18.02 g (55.63 mmol) of 1,5-diiodopentane and the solution was stirred overnight at ambient temperature. DMF was removed by high vacuum and the residue was extracted with ethyl acetate and washed with brine. The extract was dried over MgSO4, and the concentrated residue was purified by column chromatography to give the pentyl mesylate intermediate: 1H NMR (CDCl3) δ0.90(q, 6H), 1.05-2.0 (m, 17H), 2.2 (t, 1H), 2.8 (s, 6h), 3.0 (q, 2H), 3.22 (t, 2H), 3.95 (t, 2H), 4.1 (s, 1H), 5.42 (s, 1H), 6.1 (d, 1H), 6.6 (d, 1H), 6.9 (d, 2H), 7.4 (d, 2H), 7.9 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262277B1
Source datasetuspto-grants-2001_07
ORD IDord-b5fa49987762477c9fcbc71978737acb
Source noteuspto-grants-2001_07