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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507957Generated: October 31, 2026

Water → (R)-6-bromo-4-(1-cyclopropylethylamino)pyrrolo[1,2-b]pyridazine-3-carboxamide

https://huagongshe.com/reaction/1507957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Bromo-4-chloropyrrolo[1,2-b]pyridazine-3-carboxamideHCID 68291192—
Product(R)-6-bromo-4-(1-cyclopropylethylamino)pyrrolo[1,2-b]pyridazine-3-carboxamideHCID 6829175379%

Reaction Steps

A solution of 6-bromo-4-chloropyrrolo[1,2-b]pyridazine-3-carboxamide (2.0 g, 7.29 mmol), (R)-1-cyclopropylethanamine, HCl (0.975 g, 8.01 mmol) and DIPEA (2.99 mL, 17.12 mmol) in NMP (Volume: 15 mL) was heated to 100° C. for 4 hr. The reaction mixture was added 60 mL of water and stirred for 10 minutes. The solid was collected as the desired product (1.85 g, 79% yield). 1H NMR (400 MHz, CD3OD) δ 8.12 (s, 1H), 7.61 (d, J=1.8 Hz, 1H), 6.95 (d, J=1.8 Hz, 1H), 3.92 (quin, J=6.4 Hz, 1H), 1.40 (d, J=6.4 Hz, 3H), 1.18-1.05 (m, 1H), 0.65-0.49 (m, 2H), 0.41-0.30 (m, 2H). MS (ES+) m/z: 323.1, 325.1 (M+H); HPLC: 93%, retention time: 3.318 min (analytical HPLC Method B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221826B2
Source datasetuspto-grants-2015_12
ORD IDord-48b1e700320745f1a778619289cc8296
Source noteuspto-grants-2015_12