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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502473Generated: November 3, 2026

Methyl 2-methylindolizine-3-carboxylate → Methyl 2-methyl-1-nitrosoindolizine-3-carboxylate

https://huagongshe.com/reaction/502473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-methylindolizine-3-carboxylateHCID 13735249—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductMethyl 2-methyl-1-nitrosoindolizine-3-carboxylateHCID 5787229782.3%

Reaction Steps

A solution of sodium nitrite (2.2 g, 31.90 mmol) in water (10 mL) was added slowly at 0-5° C. to a stirred solution of methyl 2-methylindolizine-3-carboxylate 2 (3.9 g, 20.61 mmol) in glacial acetic acid (50 mL). After 30 min, the brown reaction mixture was poured into water. Green crystals were collected by filtration, washed with water and then dried under vacuum to give 3.7 g of expected compound; m.p.: 131-132° C. 1H NMR (CDCl3): 9.63 (d, J=7.0 Hz, 1H), 8.39 (d, J=8.5 Hz, 1H), 7.74-7.69 (m, 1H), 7.23-7.18 (m, 1H), 4.03 (s, 3H), 3.26 (s, 3H), 13C NMR (CDCl3): δ 162.5, 154.5, 141.7, 135.7, 127.9, 123.2, 118.4, 118.3, 114.5, 51.7, 11.1. Analysis calculated for C11H10N2O3: C, 60.55; H, 5.54; N, 12.84, found: C, 60.65; H, 5.60; N, 12.90.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776107B2
Source datasetuspto-grants-2010_08
ORD IDord-29429c4d0c6b431f8e812bf8458737fd
Source noteuspto-grants-2010_08