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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018151Generated: October 29, 2026

2,6-Dichlorobenzoyl chloride → HCID 12042611, compound

https://huagongshe.com/reaction/1018151

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dichlorobenzoyl chlorideHCID 78392—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 54107824HCID 54107824—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 12042611HCID 1204261199%

Reaction Steps

To a solution of 4-amino-N-[[1-[4-(methylsulfonyl)butyl]cyclopentyl]thioxomethyl]-L-phenylalanine methyl ester (19.0 mmol, 8.37 g) and 2,6-dichlorobenzoyl chloride (21 mmol, 4.4 g) in dichloromethane (90 mL) was added diisopropylethylamine (32.3 mmol, 5.6 mL) at room temperature. The solution was stirred for 15 h at which time TLC analysis of the mixture indicated the absence of starting material. Then, it was diluted with water (100 mL) and the two layers were separated. The aqueous phase was extracted with dichloromethane (100 mL) and the combined extracts were washed with brine (200 mL). The dried (MgSO4) solution was concentrated under vacuum and the residue was purified by silica gel column chromatography eluting with (hexane:ethyl acetate:dichloromethane, 1:1:1) to obtain 11.54 g (99%) of 4-[[(2,6-dichlorophenyl)carbonyl]amino]-N-[[1-[4-(methylsulfonyl)butyl]cyclopentyl]thioxomethyl]-L-phenylalanine methyl ester as a colorless solid, mp 200-202° C. HRMS: Obs. mass, 613.1367. Calcd. mass, 613.1363 (N+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479666B2
Source datasetuspto-grants-2002_11
ORD IDord-310ffa264aa742ffb2cb4ed373c155a5
Source noteuspto-grants-2002_11