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Chemical Structure| 718610-84-5 Chemical Structure| 718610-84-5

Structure of 718610-84-5

Chemical Structure| 718610-84-5

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Product Details of [ 718610-84-5 ]

CAS No. :718610-84-5
Formula : C13H23NO3S
M.W : 273.39
SMILES Code : O=C(N1CCC(CSC(C)=O)CC1)OC(C)(C)C
MDL No. :MFCD22631787

Safety of [ 718610-84-5 ]

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 [ 718610-84-5 ]

* 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 [ 718610-84-5 ]

[ 718610-84-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 718610-84-5 ]
  • [ 581060-27-7 ]
YieldReaction ConditionsOperation in experiment
With sodium tetrahydroborate; In methanol; at 0 - 20℃; for 2.16667h; Step 2 Preparation OF N-BOC-PIPERIDIN-4-YHNETHYLTHIOL. Sodium borohydride (2.2 g) was added in portions over 10 minutes to a solution of (N- Boc-piperidin-4-yl) methylthioacetate (2.2 g) in methanol (40 ml) at 0C. The mixture was allowed to warm to room temperature and was stirred for 2 hours. The reaction mixture was evaporated and the residue was dissolved in water (10 ml), citric acid (2g) was added and the mixture was extracted with dichloromethane (3X20 ml) and dried. Removal of the solvent gave the product as an orange oil, which by NMR CONTAINED-29% of the starting material. This product was used without further purification.
  • 2
  • [ 130723-13-6 ]
  • [ 718610-84-5 ]
  • [ 1245784-23-9 ]
YieldReaction ConditionsOperation in experiment
With potassium hydroxide;1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0); In toluene; at 90℃; for 18h;Inert atmosphere; Example 1; Preparation of Compound I as Illustrated by Scheme II; Step A3: Sulfide Formation from Thioacetate; To a 250 mL three-necked RBF with overhead stirring was charged with 8.6 g (31.5 mmol) of 3 in toluene from the last step, toluene (30 mL), 8.6 g (35.2 mmol-98% wt purity) of commercially available aryl bromide, 288 mg (0.31 mmol) of Pd2 dba3, 349 mg (0.62 mmol) of dppf, and 50 wt % KOH (13 mL (160 mmol)). Reaction solution was degassed under vacuum/N2 for 5 min (Vacuum and N2 was balanced at 600 torr for 5 min). Reaction was then heated to 90 C. for 18 h. Reaction was monitored by HPLC (Reaction conversion in 18 h depended on the work-up solvent from the last step. No thioalcohol (Rf 2.86) was observed during the reaction). Reaction was cooled down to 25 C. and was diluted with 35 mL (4 vol) of toluene and 70 mL of water (8 vol). Organic layer was washed with 2×50 mL of brine (6 vol). LC assay indicated 95% of LCAY and aqueous contained <1% of product Organic solution was treated with 10 mL of EtOAc and 100 wt % of Na2SO4. After stirring at rt for 10 min, 50 wt % Ecosorb C-941 and 10 wt % of PL-TMT was charged. Slurry was stirred at 45-50 C. for 1 h. After cooled to room temperature, mixture was filtered through 100 wt % of silica gel to produce compound 5. LC assay indicated 4% mass loss by carbon treatment, and metal analysis indicated a 600 ppm Pd level. Organic solution was then concentrated to 50 mL for the next step.HPLC Method
With potassium hydroxide;1,1'-bis-(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0); In toluene; at 90℃; for 18h;Inert atmosphere; Example 1; Preparation of Compound I as Illustrated by Scheme II; Step A3: Sulfide Formation from Thioacetate; To a 250 mL three-necked RBF with overhead stirring was charged with 8.6 g (31.5 mmol) of 3 in toluene from the last step, toluene (30 mL), 8.6 g (35.2 mmol-98% wt purity) of commercially available aryl bromide, 288 mg (0.31 mmol) of Pd2 dba3, 349 mg (0.62 mmol) of dppf, and 50 wt % KOH (13 mL (160 mmol)). Reaction solution was degassed under vacuum/N2 for 5 min (Vacuum and N2 was balanced at 600 torr for 5 min). Reaction was then heated to 90 C. for 18 h. Reaction was monitored by HPLC (Reaction conversion in 18 h depended on the work-up solvent from the last step. No thioalcohol (Rf 2.86) was observed during the reaction). Reaction was cooled down to 25 C. and was diluted with 35 mL (4 vol) of toluene and 70 mL of water (8 vol). Organic layer was washed with 2×50 mL of brine (6 vol). LC assay indicated 95% of LCAY and aqueous contained <1% of product Organic solution was treated with 10 mL of EtOAc and 100 wt % of Na2SO4. After stirring at rt for 10 min, 50 wt % Ecosorb C-941 and 10 wt % of PL-TMT was charged. Slurry was stirred at 45-50 C. for 1 h. After cooled to room temperature, mixture was filtered through 100 wt % of silica gel to produce compound 5. LC assay indicated 4% mass loss by carbon treatment, and metal analysis indicated a 600 ppm Pd level. Organic solution was then concentrated to 50 mL for the next step.
 

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