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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267059Generated: November 3, 2026

3-Chloropropionyl chloride → HCID 22036735, compound

https://huagongshe.com/reaction/1267059

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloropropionyl chlorideHCID 69364—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 6-amino-3,4-dihydro-1H-pyrido[4,3-b]indole-2(5H)-carboxylateHCID 22036788—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventBenzeneHCID 241—
ProductHCID 22036735HCID 2203673599%

Reaction Steps

To a solution of tert-butyl 6-amino-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indole-2-carboxylate (4.62 g, 16.08 mmol) in benzene (100 mL) was added a catalytic amount of DMAP. An inert atmosphere was created and chloropropionyl chloride (2)(1.68 mL) was added dropwise to the reaction mixture. After stirring at room temperature for 20 min, the reaction mixture was transferred to a separatory funnel containing 50% solution of sodium bicarbonate and was extracted with CH2Cl2 (3×250 mL). The combined organics were dried over Na2SO4 and concentrated in vacuo to give tert-butyl 6-[(3-chloropropanoyl)amino]-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indole-2-carboxylate as a white solid in 99% yield: 1H NMR (DMSO, 500 MHz) δ 1.38-1.53 (m, 9H), 2.75-2.99 (m, 2H), 3.65-3.78 (m, 4H), 3.88-3.97 (m, 2H), 4.53 (brs, 2H), 6.88-6.96 (m, 1H), 7.15-7.22 (m, 1H), 7.31-7.37 (m, 1H), 9.72 (brs, 1H), 10.44 (brs, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552017B1
Source datasetuspto-grants-2003_04
ORD IDord-d6ca66c5ed81429abcd25eed95671a2b
Source noteuspto-grants-2003_04