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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594211Generated: November 2, 2026

Dimethylamine → HCID 59432814, compound

https://huagongshe.com/reaction/1594211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantTriethylamineHCID 8471—
ReactantHCID 59001047HCID 59001047—
SolventDichloromethaneHCID 6344—
ProductHCID 59432814HCID 5943281471%

Reaction Steps

To a stirred solution of methanesulfonic acid 4-{[N-((1R)-1-carbamoyl-3-methyl-butyl)-N-(4-chlorobenzenesulfonyl)amino]-methyl }-benzyl ester (150 mg, 0.298 mmol) in (3 mL) CH2Cl2 at 0° C. was added 1 equivalent of Et3N, followed by dimethylamine (0.3 mL, 2 M in THF). The reaction was stirred overnight at rt. The mixture was diluted with CH2Cl2, washed with H2O, brine, dried over MgSO4, and concentrated to give an amber glass. Purification by flash chromatography (SiO2, 10% MeOH/CH2Cl2) afforded the title compound (95 mg) in 71% yield. MS (ESI), (M+H)+452.23, 1H NMR (CDCl3) δ7.94 (d, 2H, J=8.0), 7.74 (d, 2H, J=8.0), 7.63 (d, 2H, J=8.0) 7.38 (d, 2H, J=8.0), 6.23 (br s, 1H), 5.35 (br s, 1H), 4.22 (d, 1H, Jab=16), 4.14 (d, 1H, Jab=16), 3.28-3.23 (m, 3H), 2.17 (br s, 6H), 1.95 (m, 1H), 1.55 (m, 2H), 0.96 (d, 3H, J=7.0), 0.93 (d, 3H, J=7.0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300936B2
Source datasetuspto-grants-2007_11
ORD IDord-b1be563dd7ca45ada43cc88871d27068
Source noteuspto-grants-2007_11