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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842055Generated: November 3, 2026

Diisopropylethylamine → HCID 66613368, compound

https://huagongshe.com/reaction/1842055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(Tert-butoxycarbonyl)thiomorpholine-2-carboxylic acidHCID 2760619—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantMethyl 5-amino-1H-indazole-3-carboxylateHCID 28819013—
SolventDimethylformamideHCID 6228—
ProductHCID 66613368HCID 66613368—

Reaction Steps

2-(7-Aza-1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU) (1.9 g, 5 mmol) and diisopropyl ethyl amine (DIEA) (2.7 mL) was added to a suspension of 4-(tert-butoxycarbonyl)thiomorpholine-2-carboxylic acid (1.3 g, 5 mmol) in DMF (10 mL) and was stirred at room temperature for 15 minutes. Methyl 5-amino-1H-indazole-3-carboxylate (0.95 g, 5 mmol)) was added to the reaction and was stirred at room temperature for an additional 30 minutes. The reaction was quenched with water (50 mL) and extracted with ethyl acetate (3×20 mL). The extracts were combined, dried using anhydrous sodium sulfate, filtered, and concentrated in vacuo. The crude product (2.1 g) was progressed to the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946216B2
Source datasetuspto-grants-2015_02
ORD IDord-050bb8362c594cab9053cd6c1e049907
Source noteuspto-grants-2015_02