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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857899Generated: November 1, 2026

p-Methoxyphenylthionophosphine sulfide → 7-Chloro-6-pyridin-3-yl-8-thiocarbamoyl-3,4-dihydro-1H-pyrrolo[1,2-a]pyrazine-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/857899

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Methoxyphenylthionophosphine sulfideHCID 16162075—
Reactant8-carbamoyl-7-chloro-6-pyridin-3-yl-3,4-dihydro-1H-pyrrolo[1,2-a]pyrazine-2-carboxylic acid tert-butyl esterHCID 68890967—
SolventTolueneHCID 1140—
Product7-Chloro-6-pyridin-3-yl-8-thiocarbamoyl-3,4-dihydro-1H-pyrrolo[1,2-a]pyrazine-2-carboxylic acid tert-butyl esterHCID 86595871—

Reaction Conditions

Temperature80 °C

Reaction Steps

A stirred suspension of 8-carbamoyl-7-chloro-6-pyridin-3-yl-3,4-dihydro-1H-pyrrolo[1,2-a]pyrazine-2-carboxylic acid tert-butyl ester (486 mg, Reference Example 2b) in toluene (25 mL) was treated with 4-methoxyphenylthionophosphine sulfide dimer (513 mg). After stirring at 80° C. for 2 hours the reaction mixture was allowed to cool to room temperature and then evaporated. The residue was subjected to column chromatography on silica eluting with dichloromethane, then with a mixture of methanol and dichloromethane (1:99, v/v) and then with a mixture of methanol and dichloromethane (1:49, v/v) to give the title compound (129 mg) as a off white solid, m.p. 220–221° C. [Elemental Analysis: C, 54.79; H, 5.10; N, 13.86%. Calculated for C18H21ClN4O2S: C, 55.03; H, 5.39; N, 14.26%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148215B2
Source datasetuspto-grants-2006_12
ORD IDord-a0a8f5ec5cf142af830299b5b382fd82
Source noteuspto-grants-2006_12