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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085176Generated: October 25, 2026

Nicotinic Acid → Tryptamide

https://huagongshe.com/reaction/1085176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNicotinic AcidHCID 938—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantTryptamine hydrochlorideHCID 67652—
SolventPyridineHCID 1049—
ProductTryptamideHCID 6576872.5%

Reaction Steps

To a solution of 1.97 g (10 mmol) of tryptamine hydrochloride and 1.23 g (10 mmol) of nicotinic acid in 10 ml of dry pyridine at 0° C. were added 2.20 g (10.7 mmol) of dicyclohexylcarbodiimide. The reaction mixture was stirred at room temperature for 24 hrs, and the formed dicyclohexylurea was removed by filtration (2.34 g). The pyridine was removed in vacuo, and 10 ml of methanol were added to the residue. Insoluble dicyclohexylurea in methanol was removed by filtration (0.05 g). The methanol was removed in vacuo and 10 ml of methylene chloride was added to the residue. Insoluble compound in methylene chloride was removed by filtration (0.04 g). The methylene chloride was removed in vacuo and the residue was crystallized from isopropanol. Recrystallization from methanol/isopropanol gave 1.92 g (72.5%) of N-[2-(3-indolyl)ethyl]nicotinamide as pale brown plates, m.p. 150°-152° C. IR (KBr) 3280, 3050, 2940, 1646, 1526, 1412, 1302, 1102, 740, 697 cm-1. Anal. calc. for C16H15N3O: C, 72.42; H, 5.91; N, 15.84. Found: C, 72.51; H, 5.74; N, 15.77.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008257
Source datasetuspto-grants-1991_04
ORD IDord-c0a86adf53aa42fea3cccf41424af423
Source noteuspto-grants-1991_04