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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655741Generated: October 29, 2026

Water → ethyl 4-(5-chloropyrazin-2-yl)-2-[(3S,4R)-4-{[(3,4-dichloro-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}-3-methylpiperidin-1-yl]-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/655741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 2-bromo-4-(5-chloropyrazin-2-yl)-1,3-thiazole-5-carboxylateHCID 58074997—
Reactant3,4-dichloro-5-methyl-N-[(3S,4R)-3-methylpiperidin-4-yl]-1H-pyrrole-2-carboxamideHCID 59402494—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Productethyl 4-(5-chloropyrazin-2-yl)-2-[(3S,4R)-4-{[(3,4-dichloro-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}-3-methylpiperidin-1-yl]-1,3-thiazole-5-carboxylateHCID 5940254478%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of ethyl 2-bromo-4-(5-chloropyrazin-2-yl)-1,3-thiazole-5-carboxylate (Intermediate 47, 1.8 g, 5.142 mmol), and 3,4-dichloro-5-methyl-N-[(3S,4R)-3-methylpiperidin-4-yl]-1H-pyrrole-2-carboxamide (Intermediate 39, 1.47 g, 5.142 mmol) in N-methyl 2-pyrrolidinone (1 mL) was added N,N-Diisopropylethylamine (1.7 mL, 10.284 mmol) at room temperature. The reaction mixture was heated to 50° C. for 5 h. The reaction mixture was cooled to room temperature, water (60 mL) was added, the precipitated product was collected by filtration, washed with water and dried to afford 2.2 g (78%) of ethyl 4-(5-chloropyrazin-2-yl)-2-[(3S,4R)-4-{[(3,4-dichloro-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}-3-methylpiperidin-1-yl]-1,3-thiazole-5-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071605B2
Source datasetuspto-grants-2011_12
ORD IDord-99b656d06faf47e8bab3ecdfc4b32f01
Source noteuspto-grants-2011_12