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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875007Generated: October 31, 2026

Methylamine → methyl 3-chloro-4-[(methylamino)carbonyl]-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/1875007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant4-chloro-5-[(methyloxy)carbonyl]-1H-pyrrole-3-carboxylic acidHCID 68486211—
SolventDimethylformamideHCID 6228—
Productmethyl 3-chloro-4-[(methylamino)carbonyl]-1H-pyrrole-2-carboxylateHCID 6848549457.7%

Reaction Steps

To a solution of 4-chloro-5-[(methyloxy)carbonyl]-1H-pyrrole-3-carboxylic acid (0.075 g, 0.368 mmol) in DMF (1 ml) was added HATU (0.168 g, 0.442 mmol), DIPEA (0.097 ml, 0.553 mmol) and methyl amine (2M in THF) (0.276 ml, 0.553 mmol). The reaction mixture was stirred at RT overnight. Purification was accomplished by HPLC, the desired fractions collected and lypholized to afford methyl 3-chloro-4-[(methylamino)carbonyl]-1H-pyrrole-2-carboxylate (0.046 g, 57.6% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ ppm 12.39 (br. s., 1H) 7.73-7.83 (m, 1H) 7.46 (d, 1H) 3.80 (s, 3H) 2.70 (d, 3H). MS: m/z 217.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-b906425531164e3a905cdcadfde1afa3
Source noteuspto-grants-2012_11