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Dimethylformamide → HCID 21193267, compound

HRID 443275
Notes
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Reaction equation

HRID 443275 reaction equation
C(OC([N:8]1[CH2:16][CH2:15][C:11]([CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[CH:19]=2)([C:12](O)=[O:13])[CH2:10][CH2:9]1)=O)(C)(C)C.Cl.CN(C)[CH2:28][CH2:29][CH2:30]N=C=NCC.[OH2:37].ON1C2C=CC=CC=2N=N1.[Cl-].[NH4+:49].[CH:50](N(C(C)C)CC)(C)C.CN(C)[CH:61]=[O:62]>>[C:29]([O:37][C:61]([NH:49][C:12](=[O:13])[C:11]1([CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[C:20]([CH3:24])[CH:19]=2)[CH2:15][CH2:16][NH:8][CH2:9][CH2:10]1)=[O:62])([CH3:30])([CH3:50])[CH3:28]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 6228DimethylformamideHCID 25517Ammonium ChlorideHCID 81531DiisopropylethylamineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 211933671-Boc-4-(3-methylbenzyl)-4-carboxypiperidine

Product

1
HCID 21193267HCID 21193267, compound

Procedure

A mixture of N-tert-butoxycarbonyl-4-(3-methylbenzyl)-isonipecotic acid (1.02 g, 3.00 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.64 g. 3.36 mmol), 1-hydroxy-benzotriazole hydrate (0.45 g, 3.31 mmol), ammonium chloride (0.33 g, 6.15 mmol), and diisopropylethylamine (1.15 mL, 6.60 mmol) in anhydrous dimethylformamide (10 ml) was stirred at room temp. overnight. The resultant solution was concentrated under vacuum and the residue was partitioned between ethyl acetate and water. The organic extracts were combined, washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under vacuum. The residual oil was subjected to column chromatography on silica eluting with 40% ethyl acetate in hexane. Collection and concentration of appropriate fractions provided the title product.

Workup

  1. concentrationThe resultant solution was concentrated under vacuum
  2. customthe residue was partitioned between ethyl acetate and water
  3. washwashed with brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under vacuum
  7. customCollection and concentration of appropriate fractions

Sources & evidence

ORD record
ord-e525b29e10f04bd1b8ab78b2f3f0d677
Source dataset
uspto-grants-1999_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05891889

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes