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Chemical Structure| 693245-53-3 Chemical Structure| 693245-53-3

Structure of 693245-53-3

Chemical Structure| 693245-53-3

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Product Details of [ 693245-53-3 ]

CAS No. :693245-53-3
Formula : C11H17NO3
M.W : 211.26
SMILES Code : O=C(N1[C@](C2)([H])CC[C@]2([H])C1=O)OC(C)(C)C
MDL No. :MFCD32641694

Safety of [ 693245-53-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 693245-53-3 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 693245-53-3 ]

[ 693245-53-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 693245-53-3 ]
  • [ 261165-05-3 ]
YieldReaction ConditionsOperation in experiment
Product distribution / selectivity; Step 3; (1S, 3R)- (+)-3-N-BOC-Aminocyclopentane-l-carboxylic acid; Hydrolytic cleavage of Step 2 intermediate (8. 5 g, 40.26 mmol) as described in Intermediate 2, Method B, Step 2 gave the desired product as a white solid. IR and'H NMR spectra were identical with that of the racemic intermediate. [Ot] D + 12. 2 (c = 1.0, MeOH).
Hydrolytic cleavage of Step 1 intermediate (8.5 g, 40.26 mmol) as described in Intermediate 2, Method B, Step 2 gave the desired product as a white solid. IR and 1H NMR spectra were identical with that of the racemic intermediate; [a]D + 12.2 (c = 1.0, MeOH).
Step 3: (15r,3i?)-(+)-3 -N-BOC- Aminocyclopentane-1-carboxylic acid: To a stirred solution of Step 2 intermediate (8.5 g, 40.26 mmol) in THF (40 ml) was added IN sodium hydroxide (80 ml) and the mixture was stirred at 50 0C for 24 h. The reaction mixture was cooled to 0 C and acidified to pH 3.5 with 1 N hydrochloric acid. The mixture was extracted with dichloromethane (3 x 100 ml) and the combined organic extracts were washed with water (2 x 100 ml), brine (100 ml) and dried (Na2SO4). The solvent was evaporated under reduced pressure to give 8.0 g of the product as a white solid, which was identical in all respects with the product isolated by Method A.
Step 3: (15',3/?)-(+)-3-7V-BOC-Aminocyclopentane-l-carboxylic acid:; To a stirredsolution of Step 2 intermediate (8.5 g, 40.26 mmol) in THF (40 ml) was added INsodium hydroxide (80 ml) and the mixture was stirred at 50 C for 24 h. The reactionmixture was cooled to 0 C and acidified to pH 3.5 with 1 N hydrochloric acid. Themixture was extracted with dichloromethane (3 x 100 ml) and the combined organicextracts were washed with water (2 x 100 ml), brine (100 ml) and dried (Na2SC>4).The solvent was evaporated under reduced pressure to give 8.0 g of the product as awhite solid, which was identical in all respects with the product isolated by Method A.

 

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