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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1694376Erstellt: 26. Oktober 2026

Diisopropylethylamine → Methyl 4-(1-(indoline-7-carboxamido)cyclopropyl)benzoate

https://huagongshe.com/reaction/1694376

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktSodium BicarbonateHCID 516892—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
EduktN-Boc-indoline-7-carboxylic acidHCID 14977845—
EduktMethyl 4-(1-aminocyclopropyl)benzoateHCID 45140209—
LösungsmittelAcetonitrileHCID 6342—
ProduktMethyl 4-(1-(indoline-7-carboxamido)cyclopropyl)benzoateHCID 58017568—

Reaktionsschritte

1-(tert-butoxycarbonyl)indoline-7-carboxylic acid (300 mg, 1.14 mmol), HATU (475 mg, 21.2 mmol) and methyl 4-(1-aminocyclopropyl)benzoate (262 mg, 1.37 mmol) were added to acetonitrile (7.6 ml). The solution was cooled in an ice bath and DIPEA (695 ul, 3.99 mmol) was added. After 2 hr at RT, the mixture was poured into a solution of NaHCO3 (½ sat.) and washed 3 times with EtOAc. The combined organic layers were washed with brine and dried with Na2SO4. The solvent was removed and the crude mixture purified by flash chromatography on silica gel. The Boc group was removed with 1:1 TFA/DCM using the standard procedure.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08158671B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-6ccbfe3566654562ad5557ca8317821b
Quellennotizuspto-grants-2012_04