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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875009Generated: October 30, 2026

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

https://huagongshe.com/reaction/1875009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
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-[(dimethylamino)carbonyl]-1H-pyrrole-2-carboxylateHCID 6848737249.5%

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 dimethyl amine (2M in THF) (0.276 ml, 0.553 mmol) and the reaction stirred at RT for 1 h. Purification was accomplished by HPLC to afford methyl 3-chloro-4-[(dimethylamino)carbonyl]-1H-pyrrole-2-carboxylate (0.042 g, 49% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 12.40 (br. s., 1H) 7.23 (d, 1H) 3.80 (s, 3H) 2.93 (s, 6H). MS: m/z 231.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-acc59fe774714ce780319e1c84443d50
Source noteuspto-grants-2012_11