반응 #92273

ord-a7edb95cb15043609256dc7662bfbb80

반응 방정식

CCN(C(C)C)C(C)C
DIEA
Nc1cnn2ccc(N3CCC[C@@H]3c3cc(F)cc(Cl)c3)nc12
(R)-5-(2-(3-chloro-5-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-amine
O=C(n1ccnc1)n1ccnc1
CDI
Cl.OC1CNC1
azetidin-3-ol hydrochloride
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cc(F)cc(Cl)c3)nc12)N1CC(O)C1
final product
수율 74.0%
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cc(F)cc(Cl)c3)nc12)N1CC(O)C1
(R)—N-(5-(2-(3-chloro-5-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxyazetidine-1-carboxamide
수율 74.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGThe reaction was stirred overnight before it
  2. 2
    농축was concentrated
  3. 3
    기타directly purified by reverse-phase column chromatography
  4. 4
    세척eluting with 0 to 60% acetonitrile/water

실험 절차

To a DCM (0.7 mL) solution of (R)-5-(2-(3-chloro-5-fluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-amine (20 mg, 0.06 mmol, prepared as described in the following paragraph), was added CDI (20 mg, 0.12 mmol) at ambient temperature in one portion. After stirring two hours, azetidin-3-ol hydrochloride (20 mg, 0.18 mmol) was added in one portion, followed by addition of DIEA (0.032 mL, 0.18 mmol). The reaction was stirred overnight before it was concentrated and directly purified by reverse-phase column chromatography, eluting with 0 to 60% acetonitrile/water to yield the final product as a solid (29 mg, 74% yield). MS (apci) m/z=431.2 (M+H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09447104B2uspto-grants-2016_09