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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270954Generated: November 4, 2026

1-Methyl-1H-indole-2-carbonyl chloride → N-(4-{4-amino-7-[(3-pyrrolidin-1-ylpropanoyl)amino]thieno[3,2-c]pyridin-3-yl}-2-methoxyphenyl)-1-methyl-1H-indole-2-carboxamide

https://huagongshe.com/reaction/1270954

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-1H-indole-2-carbonyl chlorideHCID 12303314—
ReactantN-[4-amino-3-(4-amino-3-methoxyphenyl)thieno[3,2-c]pyridin-7-yl]-3-pyrrolidin-1-ylpropanamideHCID 18451410—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductN-(4-{4-amino-7-[(3-pyrrolidin-1-ylpropanoyl)amino]thieno[3,2-c]pyridin-3-yl}-2-methoxyphenyl)-1-methyl-1H-indole-2-carboxamideHCID 18451225—

Reaction Steps

1-Methyl-1H-indole-2-carbonyl chloride (109 mg, 0.6 mmol) in dichloromethane (2 mL) was added to N-[4-amino-3-(4-amino-3-methoxyphenyl)thieno[3,2-c]pyridin-7-yl]-3-pyrrolidin-1-ylpropanamide (0.5 mmol) in pyridine (3 mL) at about 0° C. The ice-water bath was removed and the reaction mixture was stirred at room temperature overnight. The solvent was removed and residue was purified by reverse phase preparative HPLC to give the title compound as the acetate salt (116 mg, 37%). 1H NMR (DMSO, d6) δ 1.75 (m, 4H), 1.90 (s, 3H), 2.55 (m, 6H), 2.77 (t, 2H), 3.91 (s, 3H), 4.04 (s, 3H), 5.44 (s, 2H), 7.08 (d, 1H), 7.15 (t, 1H), 7.20 (s, 1H), 7.33(t, 1H), 7.35 (s, 1H), 7.55 (s, 1H), 7.59 (d, 1H), 7.71 (d, 1H), 7.91 (s, 1H), 7.99 (d, 1H), 9.51 (s, 1H), 10.14 (s, 1H). LCMS: MH+=567.3, Rt =2.579 min. (a).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07202363B2
Source datasetuspto-grants-2007_04
ORD IDord-d511ec957847463cbcb0a17f297c5344
Source noteuspto-grants-2007_04