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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948385Generated: October 27, 2026

Diisopropylethylamine → cis(+/-)Tert-butyl-3-azido-4-{[(3,4-dichloro-5-methyl-1h-pyrrol-2-yl)carbonyl]amino}piperidine-1-carboxylate

https://huagongshe.com/reaction/1948385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTert-butyl-4-amino-3-azidopiperidine-1-carboxylateHCID 72275737—
Reactant3,4-Dichloro-5-methyl-1H-pyrrole-2-carbonyl chlorideHCID 86038394—
SolventDichloromethaneHCID 6344—
Productcis(+/-)Tert-butyl-3-azido-4-{[(3,4-dichloro-5-methyl-1h-pyrrol-2-yl)carbonyl]amino}piperidine-1-carboxylateHCID 13173033969%

Reaction Steps

Crude tert-butyl-4-amino-3-azidopiperidine-1-carboxylate (Intermediate 270, 3.3 mmol) was dissolved in anhydrous CH2Cl2 (10 ml) and DIEA (1.27 g; 1.6 ml; 9.9 mmol; 3 eq.). The solution was cooled to 0 C and 3,4-dichloro-5-methyl-1H-pyrrole-2-carbonyl chloride (736 mg; 3.5 mmol; 1.05 eq.) was added. The reaction was complete within 30 minutes. Dilute with CH2Cl2 and wash with H2O (×2), brine and dried over Na2SO4. Filter and concentrate. Purify by flash column chromatography (0-60% EtOAc/hexanes). Isolation gave 967 mg in 69% yield over the two-step sequence. LC/MS (ES−)[(M−H)+]: 415, 417 for C16H22Cl2N6O3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399489B2
Source datasetuspto-grants-2013_03
ORD IDord-d6caecf170184a9ea001b9e2b0a7715e
Source noteuspto-grants-2013_03