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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421664Generated: October 25, 2026

Tris(hydroxymethyl)aminomethane → HCID 178461736, compound

https://huagongshe.com/reaction/421664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN,N'-Di-Boc-thioureaHCID 5193990—
Reactant2-amino-9-[(2S)-2-aminopropyl]-9H-pyrido[2,3-b]indole-3-carboxamideHCID 59513644—
SolventDichloromethaneHCID 6344—
ProductHCID 178461736HCID 17846173642.2%

Reaction Steps

To a solution of 2-amino-9-[(2S)-2-aminopropyl]-9H-pyrido[2,3-b]indole-3-carboxamide (30, 100 mg, 0.350 mmol) in methylene chloride (3 mL) was added PL-DCC resin (394 mg, 0.575 mmol) and the mixture was stirred at room temperature for 15 min. N,N′-bis-tert-butoxycarbonylthiourea (112 mg, 0.406 mmol) was added and the reaction mixture was stirred at room temperature overnight. PS-trisamine resin (4.12 g, 3.6 mmol/g, 14.8 mmol) was subsequently added and the resulting mixture was stirred at room temperature overnight. The resins were removed by suction filtration and the filtrate was concentrated under reduced pressure. Purification of the crude material by reverse phase C-18 silica gel chromatography [0-70% acetonitrile in water (containing 0.1% TFA)] afforded 2-amino-9-((2S)-2-{[amino(imino)methyl]amino}propyl)-9H-pyrido[2,3-b]indole-3-carboxamide (71, 48 mg 26%). NH4OAc standard conditions. DAD Retention time=4.98 min. M+H=326.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101604B2
Source datasetuspto-grants-2012_01
ORD IDord-a3e1af1dfa554d5ca8f8948de581da0e
Source noteuspto-grants-2012_01