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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875005Generated: October 29, 2026

Diisopropylethylamine → methyl 4-(aminocarbonyl)-3-chloro-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/1875005

Reaction equation

Participants

RoleNameHCIDCharge
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 4-(aminocarbonyl)-3-chloro-1H-pyrrole-2-carboxylateHCID 6848726559%

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 DIPEA (0.097 mL, 0.553 mmol) and HATU (0.168 g, 0.442 mmol). Ammonia was bubbled through the reaction mixture for 5 min. and the reaction stirred at RT for 1 h. The crude material was purified by HPLC. The desired fractions were collected and lypholized to afford methyl 4-(aminocarbonyl)-3-chloro-1H-pyrrole-2-carboxylate (0.044 g, 59% yield) as a white solid. 1H NMR (400 MHz, DMSO-d6): δ ppm 12.40-12.56 (m, 1H) 7.54 (d, 1H) 7.29 (br. s., 1H) 7.13 (br. s., 1H) 3.80 (s, 3H). MS: m/z 203.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-c3c79e1f11aa4352a09de2dcff399c4a
Source noteuspto-grants-2012_11