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Dimethylformamide → HCID 66918650, compound

HRID 1367511
Notes
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Reaction equation

HRID 1367511 reaction equation
C(CN[C:5]([C@@H:7]1[CH2:11][C@@H:10](S(C2C=CC=CC=2)(=O)=O)[CH2:9][C@H:8]1[C:21](N1CCOCC1)=[O:22])=[O:6])#N.Cl.CN(C)CCCN=C=NCC.[OH:41][C:42]1[C:50]2N=NNC=2C=CC=1.C(N(C(C)C)C(C)C)C.Cl.[F:61][C:62]1([F:66])[CH2:65][NH:64][CH2:63]1.CN(C)C=[O:70]>>[CH2:42]([O:41][C:21]([C@@H:8]1[CH2:9][C:10](=[O:70])[CH2:11][C@H:7]1[C:5]([N:64]1[CH2:65][C:62]([F:66])([F:61])[CH2:63]1)=[O:6])=[O:22])[CH3:50]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 6

HCID 6228DimethylformamideHCID 81531DiisopropylethylamineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27582473,3-Difluoroazetidine hydrochlorideHCID 49835673HCID 49835673, compoundHCID 178418300HCID 178418300, compound

Product

1
HCID 66918650HCID 66918650, compoundYield 57%

Procedure

To a mixture of (1R,2R,4R)-4-Benzenesulfonyl-2-(morpholine-4-carbonyl)-cyclopentanecarboxylic acid cyanomethyl-amide (3 g, 15 mmol, example 1, step 1) in dimethylformamide (40 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (5.86 g, 30 mmol), hydroxybenzotriazole (3.1 g mg, 22 mmol) and ethyldiisopropylamine (15.4 mL, 90 mmol). After 45 mM, 3,3-difluoroazetidine hydrochloride (1.94 g, 15 mmol) was added and the reaction mixture was stirred for 24 h then partitioned between ethyl acetate and an aqueous saturated solution of sodium hydrogenocarbonate. The aqueous layer was extracted with ethyl acetate and the combined organic layers were washed with water then dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography on silica gel with a gradient of cyclohexane/ethyl acetate (2:1 then 1:1 v/v) as eluant to afford the title compound (2.35 g, 57%) as yellow solid. MS (EI): 276.2 (M+H)+.

Workup

  1. customthen partitioned between ethyl acetate
  2. extractionThe aqueous layer was extracted with ethyl acetate
  3. washthe combined organic layers were washed with water
  4. dry with materialthen dried over sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by flash chromatography on silica gel with a gradient of cyclohexane/ethyl acetate (2:1

Sources & evidence

ORD record
ord-f810af8d968b4aef86433c3d42827e4a
Source dataset
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07893099B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes