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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053675Generated: October 30, 2026

Methylamine → HCID 21037779, compound

https://huagongshe.com/reaction/2053675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 22042619HCID 22042619—
SolventDichloromethaneHCID 6344—
ProductHCID 21037779HCID 21037779—

Reaction Steps

0.2 g of 4-[4-(benzenesulfonyl-isobutyl-amino)-phenyl]-5,5,5-trifluoro-4-hydroxy-pent-2-ynoic acid (see Example 69; 0.439 mmol) and 0.26 mL of methylamine (2M in THF) were combined in 3 mL of CH2Cl2 at rt. 0.1 g of 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (0.527 mmol) was added. The resulting mixture was stirred at rt for 16 h. After addition of 80 mL of CH2Cl2 the resulting solution was washed with an aqueous solution of citric acid, a saturated aqueous solution of sodium bicarbonate and brine. The organic layers were dried over MgSO4, filtered and the filtrate was concentrated. The residue was purified by chromatography on silica(EtOAc:hexanes, 1:1) to give the title compound. 1H NMR (400 MHz, CDCl3) δ 0.90 (m, 6 H), 1.56 (m, 1 H), 2.91 (d, J=5.0 Hz, 3 H), 3.31 (m, 2 H), 3.72 (br s, 1 H), 6.26 (d, 5.0 Hz, 1 H), 7.11 (d, J=8.7 Hz, 2 H), 7.44-7.60 (m, 5 H), 7.64 (d, J=8.7 Hz, 2 H). Mass Spectrum (CI+) m/e=486 (M+18).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326812B2
Source datasetuspto-grants-2008_02
ORD IDord-03b3d28957894bceb619d62a84284cc3
Source noteuspto-grants-2008_02