tert-butyl [(3R)-1-(cis-2-azidocyclohexyl)pyrrolidin-3-yl]carbamate → HCID 86608974, compound

HRID 1173236Notes

Reaction equation

HRID 1173236 reaction equation
[N:1]([C@H:4]1[CH2:9][CH2:8][CH2:7][CH2:6][C@H:5]1[N:10]1[CH2:14][CH2:13][C@@H:12]([NH:15]C(=O)OC(C)(C)C)[CH2:11]1)=[N+:2]=[N-:3]>Cl.O1CCOCC1>[N:1]([C@H:4]1[CH2:9][CH2:8][CH2:7][CH2:6][C@H:5]1[N:10]1[CH2:14][CH2:13][C@@H:12]([NH2:15])[CH2:11]1)=[N+:2]=[N-:3]

Participants

3

Reactant 1

HCID 86608975tert-butyl [(3R)-1-(cis-2-azidocyclohexyl)pyrrolidin-3-yl]carbamate

Product 1

HCID 86608974HCID 86608974, compoundYield 124.5%

Reagents, catalysts & solvents 1

HCID 204431481,4-Dioxane hydrochlorideSolvent

Procedure

The mixture of tert-butyl [(3R) -1-(cis-2-azidocyclohexyl)pyrrolidin-3-yl]carbamate (0.57 g, 1.842 mmol) in 4 N HCl/dioxane (10 mL) was stirred at room temperature for 1 hour. The solution was concentrated to give 0.48 g of the title compound as HCl salt. MS (EI) calcd: (M+H)+=210.2; found: 210.2.

Workup

  1. concentrationThe solution was concentrated

Sources & evidence

ORD record
ord-a7e2dd42bce841a387ac84e0cbe9d928
Source dataset
uspto-grants-2010_11
Patent number
US07834021B2

Reaction notes

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