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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047735Generated: October 30, 2026

Diisopropylethylamine → 2-[(Isoquinoline-4-carbonyl)-amino]-indan-2-carboxylic acid

https://huagongshe.com/reaction/1047735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant5,6,7,8-Tetrahydro-1-naphthalenecarboxylic acidHCID 239604—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant2-Amino-5-methoxy-indan-2-carboxylic acid ethyl esterHCID 59314128—
SolventDimethylformamideHCID 6228—
Product2-[(Isoquinoline-4-carbonyl)-amino]-indan-2-carboxylic acidHCID 5931420982.4%

Reaction Steps

To a solution of 5,6,7,8-tetrahydro-naphthalene-1-carboxylic acid (400 mg, 2.27 mmol), 2-amino-5-methoxy-indan-2-carboxylic acid ethyl ester (639 mg, 2.72 mmol), HATU (1.3 g, 3.41 mmol) in anhydrous DMF (15 mL) is added DIPEA (563 μL, 3.41 mmol). The resulting solution is stirred at RT overnight. After the removal of DMF in vacuo, the residue is dissolved in EtOAc (50 mL) and washed with water (1×10 mL) and brine (2×10 mL). The organic layer is dried over anhydrous Na2SO4 and concentrated in vacuo. The residue is purified by flash column chromatography (115 g silica gel, gradient elution: 5%-40% EtOAc in heptane) to give a pure product (52) as white solid (622 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569535B2
Source datasetuspto-grants-2013_10
ORD IDord-9b8a1f4e2e014ef58f14d2427f24b174
Source noteuspto-grants-2013_10