Hydrochloric Acid → HCID 68508753, compound

HRID 1715122Notes

Reaction equation

HRID 1715122 reaction equation
[CH2:1]([O:4][C:5]([C:7]1[CH:28]=[CH:27][C:10]2[N:11]([CH:14]3[CH2:19][CH2:18][N:17](C(OC(C)(C)C)=O)[CH2:16][CH2:15]3)[N:12]=[N:13][C:9]=2[CH:8]=1)=[O:6])[CH:2]=[CH2:3].[ClH:29]>O1CCOCC1>[ClH:29].[ClH:29].[CH2:1]([O:4][C:5]([C:7]1[CH:28]=[CH:27][C:10]2[N:11]([CH:14]3[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]3)[N:12]=[N:13][C:9]=2[CH:8]=1)=[O:6])[CH:2]=[CH2:3]

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 68509182HCID 68509182, compound

Product 1

HCID 68508753HCID 68508753, compound

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent2×

Procedure

A solution of 1-(1-tert-butoxycarbonyl-piperidin-4-yl)-1H-benzotriazole-5-carboxylic acid allyl ester (1.40 g, 3.62 mmol) in dioxane (20 mL) and 4 M HCl in dioxane (20 mL) was stirred at rt for 2 h. The solvent was removed under reduced pressure and the crude product used in the consecutive step without further purification assuming quantitative deprotection and formation of the dihydrochloride salt. MS (ISP): 287.3 [M+H]+.

Workup

  1. customThe solvent was removed under reduced pressure
  2. customthe crude product used in the consecutive step without further purification

Sources & evidence

ORD record
ord-fbc10d2d207f4d0bb2b1ac1d2a06c296
Source dataset
uspto-grants-2010_09
Patent number
US07799806B2

Reaction notes

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