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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117942Generated: November 1, 2026

Ammonium Chloride → HCID 86595609, compound

https://huagongshe.com/reaction/2117942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 21914852HCID 21914852—
Reactant(S)-N,N-DiMethyl-2-pyrrolidinecarboxaMide HClHCID 66702040—
SolventDichloromethaneHCID 6344—
ProductHCID 86595609HCID 86595609—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of the compound obtained in Step 2 (200 mg) in dichloromethane (6 mL) were added (2S)-2-(N,N-dimethylaminocarbonyl)pyrrolidine hydrochloride and diisopropylethylamine (0.27 ml) at 5° C. The mixture was stirred at 5° C. for 10 min. Then sodium triacetoxyborohydride (327 mg) was added, and the mixture was stirred for 3 hrs. aq. NH4Cl was added, and the mixture was extracted with dichloromethane. The organic layer was dried over MgSO4. The layer was concentrated under reduced pressure. The resulting crude mixture was purified by silica gel column chlomatography with mixed solvent (dichloromethane/methanol=15/1) as an eluent to give tert-butyl(4-{2-[2-(acetylamino)-5-({(2S)-2-[(N,N-dimethylamino)carbonyl]-1-pyrrolidinyl}methyl)-1,3-thiazol-4-yl]ethyl}phenyl)carbamate as a pale yellow amorphous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442715B2
Source datasetuspto-grants-2008_10
ORD IDord-b0901af53eeb4d9882e9ca01c9fa23d5
Source noteuspto-grants-2008_10