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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485890Generated: October 31, 2026

Diisopropylethylamine → HCID 90040593, compound

https://huagongshe.com/reaction/1485890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(tert-Butoxycarbonyl)-L-cyclohexylglycineHCID 7004938—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 131736761HCID 131736761—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 90040593HCID 9004059391.1%

Reaction Steps

To a solution of (S)-1,2,3,4-tetrahydro-isoquinoline-1-carboxylic acid (2,6-difluoro-phenyl)-amide trifluoroacetate (52 mg, 129 μmol, Eq: 1.00), (S)-2-(tert-butoxycarbonylamino)-2-cyclohexylacetic acid (33.3 mg, 129 μmol, Eq: 1.00) and HATU (54.1 mg, 142 μmol, Eq: 1.1) in DMF (300 μL) at 0° C. was added DIEA (50.1 mg, 67.7 μL, 388 μmol, Eq: 3). The reaction was stirred at RT for 1 h diluted with water and extracted with EtOAc. The combined organics were washed with water, brine, dried with MgSO4 and concentrated in vacuo. The crude material was purified by flash chromatography to give {(S)-1-cyclohexyl-2-[(S)-1-(2,6-difluoro-phenylcarbamoyl)-3,4-dihydro-1H-isoquinolin-2-yl]-2-oxo-ethyl}-carbamic acid tert-butyl ester (62 mg) as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422332B2
Source datasetuspto-grants-2016_08
ORD IDord-cd3fedfee75846e0a350dbc46d6f8afa
Source noteuspto-grants-2016_08