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[ CAS No. 138108-72-2 ] {[proInfo.proName]}

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Chemical Structure| 138108-72-2
Chemical Structure| 138108-72-2
Structure of 138108-72-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 138108-72-2 ]

CAS No. :138108-72-2 MDL No. :MFCD03094725
Formula : C10H19NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :HKIGXXRMJFUUKV-MRVPVSSYSA-N
M.W : 201.26 Pubchem ID :1514340
Synonyms :
Chemical Name :(R)-tert-Butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylate

Calculated chemistry of [ 138108-72-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.9
Num. rotatable bonds : 4
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 57.75
TPSA : 49.77 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.95 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.72
Log Po/w (XLOGP3) : 0.82
Log Po/w (WLOGP) : 0.85
Log Po/w (MLOGP) : 0.86
Log Po/w (SILICOS-IT) : 0.65
Consensus Log Po/w : 1.18

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.34
Solubility : 9.19 mg/ml ; 0.0457 mol/l
Class : Very soluble
Log S (Ali) : -1.45
Solubility : 7.19 mg/ml ; 0.0357 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.83
Solubility : 29.8 mg/ml ; 0.148 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.65

Safety of [ 138108-72-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 138108-72-2 ]

* 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 [ 138108-72-2 ]

[ 138108-72-2 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 114214-69-6 ]
  • [ 138108-72-2 ]
  • [ 199174-24-8 ]
YieldReaction ConditionsOperation in experiment
73% Resolution of racemate; Racemic l-t-butoxycarbonylpyrrolidine-3-methanol (15 g,74.53 mmol) was chromatographed on a chiral column[ChiralPak AD 8 X 25 cm; 2.5% of (6% MeOH/94% EtOH); 400mL/min; UV: 210 nm] to give l-t-butoxycarbonylpyrrolidine-3-methanol:Isomer I (Rt: 8.81 min, ChiralPak AD 4.6 X 250 mm; 1.0mL/min; UV: 210 nm) (6.35 g, 42%, 94% ee) andIsomer II (Rt: 9.68 min)' (6.43 g, 43%, 90% ee) .Isomer I: FIA-MS, m/e: 202.2 (rrH-1) .Isomer II: FIA-MS, m/e: 202.2 (m+1).
  • 2
  • [ 1123786-71-9 ]
  • [ 138108-72-2 ]
  • [ 199174-24-8 ]
  • 3
  • [ 138108-72-2 ]
  • [ 204688-60-8 ]
  • 4
  • [ 32315-10-9 ]
  • [ 145742-50-3 ]
  • [ 138108-72-2 ]
  • tert-butyl (3R)-3-[(2-chloro-4-formyl-5-methoxyphenyl)carbamoyloxymethyl]pyrrolidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
<strong>[145742-50-3]4-amino-5-chloro-2-methoxybenzaldehyde</strong> (3a) (462 mg, 2.49 mmol) was dissolved in 49 toluene (15 ml), 50 triethylamine (630 mg, 6.22 mmol) was added thereto, and then 51 triphosgene (554 mg, 1.87 mmol) was added under N2 protection, followed by a reaction at 120C for 1 hour. After cooling to room temperature, Reaction Solution 1 was obtained. 44 Tert-butyl (3R)-3-(hydroxymethyl)pyrrolidine-1-carboxylate (4B) (500 mg, 2.49 mmol) was dissolved in 13 tetrahydrofuran (15 ml), to which triethylamine (630 mg, 6.22 mmol) and then Reaction Solution 1 were added, followed by a reaction at 85C for 3 hours. The reaction solution was cooled to room temperature, and water (50 ml) was added thereto, which was extracted with ethyl acetate (100 mL×2). The organic phases were combined, dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure, to obtain 46 tert-butyl (3R)-3-[(2-chloro-4-formyl-5-methoxy-phenyl)carbamoyloxymethyl] pyrrolidine-1-carboxylate (4C) as a brown liquid, which was directly used in the next step without purification. LCMS m/z =451.4[M+39].
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