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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162641Generated: October 29, 2026

Ammonium Chloride → HCID 68646427, compound

https://huagongshe.com/reaction/1162641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58748273HCID 58748273—
CatalystTitanium isopropoxideHCID 11026—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 68646427HCID 68646427—

Reaction Conditions

Temperature40 °C

Reaction Steps

35.2 A solution of 500 mg (S)-3-[(5-chloro-thiophene-2-carbonyl)-amino]-4-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester in 20 ml EtOH was treated with 155 mg ammonium chloride, 0.49 ml Hünig's base and 0.86 ml tetraisopropyl orthotitanate. The reaction mixture was stirred for 5 hrs at 40° C. Then it was cooled to 0° C., treated with 110 mg NaBH4 and stirred at r.t. overnight. The mixture was diluted with EtOAc and washed with H2O. The organic layer was dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography (silica gel, gradient: CH2Cl2->CH2Cl2/MeOH 9:1) to give 180 mg (S)-3-amino-4-[(5-chloro-thiophene-2-carbonyl)-amino]-pyrrolidine-1-carboxylic acid tert-butyl ester as yellow solid. MS 344.3 ([M−H]−)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820699B2
Source datasetuspto-grants-2010_10
ORD IDord-a906de0c652b4c3ab6b3062fe3a28279
Source noteuspto-grants-2010_10