Ethyl(R)-1-boc-nipecotate

Name: Ethyl(R)-1-boc-nipecotate
SKU: ACM194726404
Rating: 5 (1 reviews)

CAS

194726-40-4

Catalog Number

ACM194726404

Category

Other Products

Molecular Weight

257.33

Molecular Formula

C₁₃H₂₃NO₄

COA MSDS SDS Spec Sheet

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Specification

Synonyms

194726-40-4, Ethyl (R)-1-Boc-nipecotate, (R)-(-)-N-BOC-NIPECOTIC ACID ETHYL ESTER, (R)-1-BOC-piperidine-3-carboxylic acid ethyl ester, AG-E-42328, (R)-1-tert-Butyl 3-ethyl piperidine-1,3-dicarboxylate, Ethyl (R)-N-Boc-piperidine-3-carboxylate, (R)-1-Boc-3-piperidinecarboxylate ethyl ester, (R)-ETHYL N-BOC-PIPERIDINE-3-CARBOXYLATE, (R)-1-(tert-Butyl) 3-ethyl 1,3-piperidinedicarboxylate, Ethyl (3R)-1-tert-butoxycarbonyl-3-piperidinecarboxylate, (R)-1-(tert-Butoxycarbonyl)-piperidine-3-carboxylic acid ethyl ester, AC1LTTIY, PubChem11374, (R)-1-Boc-Piperidine-3-CarboxylicAcidEthylEster, SureCN792692, CTK4E1592, ETHYL 1-BOC-D-NIPECOTATE, MolPort-003-982-318, ACT09197

IUPAC Name

1-O-tert-butyl 3-O-ethyl (3R)-piperidine-1,3-dicarboxylate

SMILES

CCOC(=O)C1CCCN(C1)C(=O)OC(C)(C)C

InChI Key

YCXCRFGBFZTUSU-SNVBAGLBSA-N

Boiling Point

323.9ºC at 760 mmHg

Density

1.077

Exact Mass

257.16300

H-Bond Acceptor

H-Bond Donor

Upstream Synthesis Route 1

75-03-6
163438-09-3

194726-40-4

Reference: [1] Patent: WO2014/135931, 2014, A1, . Location in patent: Page/Page column 10

Upstream Synthesis Route 2

24424-99-5
25137-01-3

194726-40-4

Reference: [1]Bioorganic and Medicinal Chemistry Letters,2002,vol. 12,p. 3235 - 3238
[2]Journal of Medicinal Chemistry,2009,vol. 52,p. 610 - 625
[3]Bioorganic and Medicinal Chemistry Letters,2009,vol. 19,p. 2829 - 2834
[4]Patent: US6335324,2002,B1 .Location in patent: Page column 253

Downstream Synthesis Route 1

24424-99-5
194726-40-4

163438-09-3

Reference: [1] Patent: US6645980, 2003, B1,

Downstream Synthesis Route 2

194726-40-4

163438-09-3

Reference: [1] Journal of Medicinal Chemistry, 2009, vol. 52, # 3, p. 610 - 625

Downstream Synthesis Route 3

194726-40-4

194726-46-0

Reference: [1]European Journal of Medicinal Chemistry,2002,vol. 37,p. 487 - 501

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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