Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632968Generated: October 31, 2026

Methyl 4-(4-(tert-butoxycarbonylamino)phenyl)-1-methyl-1H-pyrrole-2-carboxylate → Methyl 4-(4-aminophenyl)-1-methyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/632968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-(4-(tert-butoxycarbonylamino)phenyl)-1-methyl-1H-pyrrole-2-carboxylateHCID 67253196—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 4-(4-aminophenyl)-1-methyl-1H-pyrrole-2-carboxylateHCID 58326676—

Reaction Steps

5 (1 g, 3.027 mmol) was dissolved in a small volume of MeOH and 4M HCl in dioxane (15 mL) was added slowly to the stirring solution. The reaction mixture was stirred for 6 hours at which point TLC showed completion of reaction. Excess solvent was evaporated under vacuum to obtain a brown coloured solid 7. The solid product was subjected to flash chromatography (n-hexane/EtOAc 9:1) to give pure 7 (065 g, 94.2%). IR (FTIR, vmax/cm−1): 3366, 2987, 1688, 1629, 1566, 1422, 1372, 1262, 1181, 1103, 1067, 951, 821, 784, 756; 1H-NMR (400 MHz, CDCl3): δ 7.28 (2H, d, J=8.4 Hz), 7.11 (1H, d, J=2.0 Hz), 6.96 (1H, d, J=2.0 Hz), 6.68 (d, 2H, J=8.0 Hz), 3.94 (s, 3H), 3.83 (s, 3H); 13C-NMR (100 MHz, CDCl3): δ 161.7, 144.7, 126.2, 125.4, 125.2, 115.5, 114.4, 51.0, 36.8; EIMS m/z (+EI) calc. for C13H14N2O2 (M)+ 230.26. found 231.1 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321774B2
Source datasetuspto-grants-2016_04
ORD IDord-2ac424897ce44562bce734edfe9c74de
Source noteuspto-grants-2016_04