tert-Butyl 3-(2-oxo-5-(thiophene-2-carboximidamido)indolin-3-yl)pyrrolidine-1-carboxylate

An aromatic ester, C22H26N4O3S, 426.542 g/mol.

Organic — aromatic ester

Identifiers

Molecular formula: C₂₂H₂₆N₄O₃S
Molecular weight: 426.542 g/mol
Exact mass: 426.172562 g/mol
SMILES: CC(C)(C)OC(=O)N1CCC(C2C(=O)Nc3ccc(NC(=N)c4cccs4)cc32)C1
InChI: InChI=1S/C22H26N4O3S/c1-22(2,3)29-21(28)26-9-8-13(12-26)18-15-11-14(6-7-16(15)25-20(18)27)24-19(23)17-5-4-10-30-17/h4-7,10-11,13,18H,8-9,12H2,1-3H3,(H2,23,24)(H,25,27)
InChIKey: YSPWDMZYVQQKQX-UHFFFAOYSA-N

Open in ReactionLens Use in reaction prediction

Calculated properties

Derived from the structure, not from a sample; kept apart from the measurements above.

logP: 4.4783calculated · chemistry engine; Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area: 94.52 Å²calculated · chemistry engine; Surface area from polar atoms; relates to how easily a molecule crosses membranes.
H-bond donors: 3calculated · chemistry engine; Atoms that can donate a hydrogen bond.
H-bond acceptors: 5calculated · chemistry engine; Atoms that can accept a hydrogen bond.
Rotatable bonds: 3calculated · chemistry engine; Single bonds the molecule can freely twist around.
Molar refractivity: 118.4971 cm³/molcalculated · chemistry engine; Relates to the molecule's polarisability.
Fraction sp³ carbons: 0.4091calculated · chemistry engine; Share of carbon atoms with tetrahedral bonding.
QED drug-likeness: 0.4982calculated · chemistry engine; Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

C Carbon22 atoms · 61.9% by mass
N Nitrogen4 atoms · 13.1% by mass
O Oxygen3 atoms · 11.3% by mass
S Sulfur1 atom · 7.5% by mass
H Hydrogen26 atoms · 6.1% by mass

Percentages are of the molecular weight above, worked out the same way the molar mass calculator does it.

Structure

Heavy atoms, hydrogen excluded: 30
Total atoms, hydrogen included: 56
Rings: 4
Aromatic rings: 2
Stereocentres: 2
Formal charge: 0

Functional groups

Ester
A carbonyl bonded to an oxygen that links to another carbon.
Amide
A carbonyl bonded directly to nitrogen.
Ether
An oxygen bridging two carbons.
Secondary aromatic amine
A nitrogen bonded to an aromatic ring, one other carbon and one hydrogen.
Aromatic ring
A flat six-membered ring with delocalised electrons.
Aromatic ring (five-membered)
A flat five-membered ring with delocalised electrons, such as furan, thiophene or pyrrole.

Matched by structural pattern, not by a measurement.

The molecule in three dimensions

Rotate and inspect the atoms. Loaded only when you ask, so the page stays light.

The drawing above is a diagram of what is bonded to what. A molecule is not flat, and the model here is one low-energy shape generated from the connectivity — useful for seeing which groups can reach each other, and not a measured structure. A real sample is a population of conformations, interconverting.

Reactions it appears in

No documented reaction with a written procedure and a source involves tert-Butyl 3-(2-oxo-5-(thiophene-2-carboximidamido)indolin-3-yl)pyrrolidine-1-carboxylate yet.

Structurally related

Nothing structurally close to tert-Butyl 3-(2-oxo-5-(thiophene-2-carboximidamido)indolin-3-yl)pyrrolidine-1-carboxylate has a page here yet.

Where these values came from

chemistry engine
structure perception

No matching record was found in the currently indexed sources (reference compound database)..

What this page does not claim

Identifiers are copied from the source record, measured values are reported as published, and calculated values are marked as calculated. Nothing here is a hazard, purity or handling assessment — how the library is checked.