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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446974Generated: October 26, 2026

Aniline → 3-Phenylcarbamoyl-hexahydro-pyrrolo[3,2-b]pyrrole-1,4-dicarboxylic acid 1-benzyl ester 4-tert-butyl ester

https://huagongshe.com/reaction/446974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
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—
ReactantHexahydro-pyrrolo[3,2-b]pyrrole-1,3,4-tricarboxylic acid 1-benzyl ester 4-tert-butyl esterHCID 67216716—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-Phenylcarbamoyl-hexahydro-pyrrolo[3,2-b]pyrrole-1,4-dicarboxylic acid 1-benzyl ester 4-tert-butyl esterHCID 6728127569.5%

Reaction Steps

A solution of 36 (500 mg, 1.28 mmol) in NMP (7 mL) was cooled to 0° C. and treated with HATU (511 mg, 1.34 mmol) and DIPEA (0.33 mL, 1.92 mmol) followed in 15 min by the addition of aniline (0.14 mL, 1.54 mmol). The reaction mixture was allowed to warm to ambient temperature. After 3 h, the solution was diluted with EtOAc, washed with H2O, 1M HCl, H2O, sat NaHCO3, brine, dried over anhydrous Na2SO4, filtered and concentrated to afford 37 (414 mg) as a white foam that was used without further purification. Mass spectrum, m/z [466.4] (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481495B2
Source datasetuspto-grants-2013_07
ORD IDord-6fd45f0b37ab42ada2d776f9f12ab354
Source noteuspto-grants-2013_07