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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081126Generated: November 3, 2026

Diisopropylethylamine → HCID 86636566, compound

https://huagongshe.com/reaction/2081126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 57437882HCID 57437882—
ReactantHCID 57463496HCID 57463496—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86636566HCID 86636566163.7%

Reaction Steps

(2S,4R)-1-(tert-butoxycarbonyl)-4-(4-chloroisoindoline-2-carbonyloxy)pyrrolidine-2-carboxylic acid 26 (0.35 g, 0.852 mmol), (1R,2S)-1-amino-2-cyclopropyl-N-(cyclopropylsulfonyl)cyclopropanecarboxamide hydrochloride 25 (0.287 g, 1.02 mmol) and HATU (0.389 g, 1.02 mmol) were dissolved in DriSolve DMF (8.5 mL), and cooled in an ice bath. DIEA (d 0.742) (0.445 ml, 2.56 mmol) was then added to reaction drop-wise. The reaction was allowed to warm up to rt slowly and stirred overnight. After reaching completion, the reaction was diluted with water (120 mL) and extracted with EtOAc (3×150 mL). The combined organic extract was washed with 0.5 N HCl (200 mL), brine (150 mL) and dried over Na2SO4. Removal of solvent yielded the crude product as a light yellowish foamy solid, which was purified by reverse phase chromatography (eluent: 5 to 95% MeCN/water), giving pure desired product as a white solid (0.40 g, 70% yield). LCMS (APCI+): 537.2 (MH+−Boc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932277B2
Source datasetuspto-grants-2011_04
ORD IDord-6cb1c2a6c9144d6692d476f0a5045379
Source noteuspto-grants-2011_04