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Home > Encyclopedia > 6-Amino-2-aza-spiro[3.3]heptane-2-carb...

6-Amino-2-aza-spiro[3.3]heptane-2-carb...

6-Amino-2-aza-spiro[3.3]heptane-2-carb... structure

6-Amino-2-aza-spiro[3.3]heptane-2-carb... 

structure

6-Amino-2-aza-spiro[3.3]heptane-2-carb... Basic Attributes

212.2887

212.15200

1592732-453-0

DTXSID80677370

2933990090

Characteristics

55.6

0.6

115℃

Safety Information

P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, P501

H302

|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 2 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

6-Amino-2-aza-spiro[3.3]heptane-2-carb... Use and Manufacturing

To a mixture of HATU (99 mg, 0.26 mmol) and 2-(4-chloro-3-fluoro-phenoxy)acetic acid (48 mg, 0.24 mmol) in DMF (5 mL) was added tert-butyl 6-amino-2-azaspiro[3.3jheptane-2-carboxylate (50 mg, 0.24 mmol) and Na2CO3 (50 mg, 0.47 mmol), and the mixture was stirred at 20 C for 16 h. The mixture was poured into ice-water (15 mL) and extracted with EtOAc (3 x 5 mL). The combined organic phases were washed with brine (3 x 5 mL), dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by prep-TLC (Si02, PE:EtOAc = 3:1) to provide desired compound. LC-MS mlz: = 343.1, 345.1 [M+H-56j. 'H-NMR (400 MHz, CDC13): oe 7.34 (t, J= 8.6 Hz, 1H), 6.76 (dd, J= 2.8, 10.3 Hz, 1H), 6.67 (td, J = 1.4, 8.9 Hz, 1H), 6.53 (br d, J= 7.4 Hz, 1H), 4.42(s, 2H), 4.40-4.33 (m, 1H), 3.98 (s, 2H), 3.87 (s, 2H), 2.64 (ddd, J=2.9, 7.5, 10.0 Hz, 2H), 2.13 (dt, J= 2.9, 9.3 Hz, 2H), 1.44 (s, 9H)6-Amino-2-Boc-2-azaspiro[3.3]heptane (504 mg, 2.37 mmol), 3, 6-dichloropyridazine (884 mg, 5.93 mmol) and DIPEA (1.24 mL, 7.12 mmol) were dissolved in t-BuOH (3 mL) in a sealed vial, which was heated to 100 C overnight, after which time the reaction mixture was cooled to r.t. and diluted with DCM and sat. NaHCO3. The aqueous layer was extracted with DCM, and the combined organic extracts were filtered through a phase separator and concentrated. The crude residue was purified by column chromatography (hexanes/EtOAc) to give the title compound as a white solid (335 mg, 44%).1H-NMR (400 MHz, CDCl3) 7.17 (d, J = 9.2, 1H), 6.56 (d, J = 9.2, 1H), 4.79 (br, 1H), 4.25- 4.16 (m, 1H), 3.99 (s, 2H), 3.89 (s, 2H), 2.76- 2.71 (m, 2H), 2.10- 2.03 (m, 2H), 1.43 (s, 9H). ES-MS [M+H]+ = 269.4 (minus t-butyl).

Computed Properties

Molecular Weight:212.29
XLogP3:0.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:212.152477885
Monoisotopic Mass:212.152477885
Topological Polar Surface Area:55.6
Heavy Atom Count:15
Complexity:269
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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