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Hydrochloric Acid → (3-Aminomethyl-5-chloro-4-fluoro-benzyl)-diethyl-amine

HRID 1527490
Notes
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Reaction equation

HRID 1527490 reaction equation
C(OC(=O)[NH:7][CH2:8][C:9]1[CH:14]=[C:13]([CH2:15][N:16]([CH2:19][CH3:20])[CH2:17][CH3:18])[CH:12]=[C:11]([Cl:21])[C:10]=1[F:22])(C)(C)C.Cl>CO.O1CCOCC1>[NH2:7][CH2:8][C:9]1[CH:14]=[C:13]([CH:12]=[C:11]([Cl:21])[C:10]=1[F:22])[CH2:15][N:16]([CH2:19][CH3:20])[CH2:17][CH3:18]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 313Hydrochloric AcidHCID 68283941(3-Chloro-5-diethylaminomethyl-2-fluoro-benzyl)-carbamic acid tert-butyl ester

Product 1

HCID 68284257(3-Aminomethyl-5-chloro-4-fluoro-benzyl)-diethyl-amine

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 312751,4-DioxaneSolvent

Procedure

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

To a mixture of (3-chloro-5-diethylaminomethyl-2-fluoro-benzyl)-carbamic acid tert-butyl ester (115 mg, 0.33 mmol) in MeOH (1 mL) was added a solution of 4N HCl in dioxane (3 mL). The reaction mixture was stirred for 2 h at ambient temperature and the solvent was removed in vacuo to give the title compound. MS (LC/MS): 245.0 [M]+; tR (HPLC conditions c): 2.13 min.

Workup

  1. customthe solvent was removed in vacuo

Sources & evidence

ORD record
ord-ad3bd1ada82b48fbb69ad3eab7bddbc6
Source dataset
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09085555B2

Reaction notes

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